AIR OXYGEN BLENDER Instruction Manual Rev 0222322

ADDENDUM 1- Low Flow Selector Knob A low flow selector knob has been installed on some of the Bio-Med Devices Blenders (standard on units mounted on the Crossvent ventilators) in lieu of the right side output port. This enables the user to maintain accurate concentrations when using the bottom or left outputs for all flows within the specification of the blender with a simple turn of the knob.

A label attached to the side of the blender indicates how to position the knob for accurate concentrations at settings less than or greater than the flow rate indicated. The knob must be pushed in prior to turning.

ADDENDUM 2- Permanently Mounted Flowmeters Several blenders, including the NEO2 BLEND series, are offered with flowmeters mounted on the right side of the blender. In most cases, this flowmeter is mounted to a uniquely designed rotating switch that is used in the same manner as the knob described in Addendum 1. Any time these blenders are used in a flow range requiring the bleed to be active (see the Flow Table in Section 4), rotating this flowmeter as described below will activate the bleed as well as the flowmeter. Even if the flowmeter is not to be used, positioning it vertically so the bleed is active allows the blender to be used with its lower flows.

The flow rate for these flowmeters should be set using the center of the ball. RIGHT SIDE FLOWMETER & LOW FLOWS The right side flowmeter and the blender bleed are inactive when the flowmeter is angled towards the front of the blender. To activate it and initiate the required bleed for lower flows, push the flowmeter in towards the side of the blender and then rotate it clockwise (towards the back) to its vertical position. The internal bleed will now be active and the flow rate may be set using the knob on the flowmeter. As long as the flowmeter is in this position, any output port can be used for low flows even if the flowmeter itself is not being used. To return the flowmeter and bleed to its off (inactive) state, return it to its angled position by pushing it in and rotating it counterclockwise (towards the front).

LEFT SIDE FLOWMETER CAUTION: The flowmeter on the left side is stationary. Do not try to turn it. If the flowmeter on the left side is to be used for flows requiring a bleed for accuracy (see the Flow Table in Section 4), be sure the knob (refer to Addendum 1) or right-side flowmeter (see above) is set properly.

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ADDENDUM 3- Dial Flowmeters Flowmeters offered by Bio-Med Devices that are set by rotating a dial on top of the flowmeter are not pressure compensating. Not pressure compensating means that in order for the flowmeter to accurately deliver the flow rate indicated by the dial, the supply pressure to the flowmeter input must at all times be the same pressure the flowmeter is rated for. If the flowmeter is rated for a 50 PSI supply pressure, then 50 PSI is required at the input in order for the set flow rates to be accurate. In practice, these flowmeters are often connected to Air/Oxygen blenders and by doing so, the blender then becomes the supply source to the flowmeters. WARNING: Before use on a patient, the oxygen concentration of the delivered gas should be checked at the setting intended for use. A separate, calibrated oxygen monitor (complying with ISO 80601-2-55) must be used whenever the blender is used on a patient.

It is important to understand that although there may be 50 PSI at the input to the blender, this does not mean there is always 50 PSI at the output of the blender (input to the flowmeters). As flow increases, there is an inherent reduction in pressure at the blender’s output due to the restrictive nature, albeit slight, of the blender. Therefore, there is less than 50 PSI at the input to the flowmeters in this situation and flow accuracy suffers. As the input pressure to the flowmeter decreases, so does the flow rate relative to its setting. Another variable to note with Air/Oxygen blenders is the concentration setting. As the concentration setting is varied, so varies the restrictive nature of the blender, further affecting the blender’s output pressure. Think in terms of hot and cold water faucets. When you have just the hot or just the cold faucet turned on, the water pressure is less than when you have both faucets turned on. The blender acts in a similar fashion. More pressure is available when you are mixing air and oxygen than when you are just using one or the other. Still another variable is the pressure downstream from the flowmeter. Since flow is created by one pressure being greater than another, it stands to reason that the less difference there is between the pressures, the less flow there will be. This downstream pressure may be very low, but needs to be mentioned. So what is stated above are some of the variables that need to be considered when flowmeters that are not pressure compensating are used with blenders. Any additional device, other than the flowmeter, that delivers flow from the blender, be it a ventilator or other device, must also be taken into account. The flow this additional device is delivering exacerbates the situation so that device should be turned off when using the flowmeters.

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1. WARNINGS, CAUTIONS AND NOTES WARNINGS Never leave a ventilator patient unattended, or without remote monitoring. If the pressure of the oxygen or air gas source increases or decreases resulting in a 20 PSI* (138 kPa) difference (*30 PSI [207 kPa] in the case of overseas devices and those manufactured for Draeger / Hill Rom / Air-Shields), the alarm will sound. This will affect the blender’s output flow and oxygen concentration. The blender alarm will sound if the air or oxygen gas source fails. This indicates to the user that the oxygen concentration or flow may not be accurate. A physician must determine the correct FIO2 setting. The blender must not be exposed to extremely high temperatures, as in the case of steam autoclaving (which could reach 145° F / 63° C). The alarm should not be obstructed, removed or tampered with in any way. The blender is designed to operate from a 50 psig (345 kPa) source of air and oxygen. Before use on a patient, the oxygen concentration of the delivered gas should be checked at the setting intended for use. A separate, calibrated oxygen monitor (complying with ISO 80601-2-55) must be used whenever the blender is used on a patient. The bleed port on the bottom of the blender must not be covered at any time. Some special order blenders may not have a bleed when using the right side outlet. When this is the case, the flow specifications for “flow without bleed” apply to the auxiliary right side outlet. The factory-installed Air and Oxygen gas supply fittings, which contain essential check valves and filters, must not be substituted with any other parts not approved by Bio-Med Devices. Doing so may cause gas supply contamination due to back-flow. This blender is not suitable for use with Oxygen 93. Bleed oxygen flow can cause ignitions. Do not attempt to service or perform maintenance while the blender is in use. Only qualified medical personnel should operate the Blender. CAUTIONS Moisture or dirt can affect the operation of the blender; a clean dry gas source must be used at all times. The air must meet “USP grade” compressed air standard (formerly ANSI Z86.1-1973 grade F) and at 75 PSI (517 kPa) water vapor content cannot exceed -1-

a dew point of 5° F (2.8° C) below the lowest ambient temperature to which the blender and accessories are exposed. The oxygen should be “medical oxygen” per FDA terminology, that is, at least 99.0% pure. Both gases must contain < 37.5 milligrams of water per cubic meter of gas ( mg 3 ) or < 50 ppm H2O. Nm

A water trap assembly and filter must be used to avoid malfunction should water accidentally get into the gas supply sources. Do not use in an MRI room unless the blender has been built by Bio-Med Devices to be used for such an environment. This will be indicated by “MRI” on the blender front plate, and an MR-conditional label on the case. The flowmeter on the left side of the NEO2 BLEND is stationary. Do not try to turn it. If the blender does not pass the performance test, do not place the unit into service; call your dealer or service representative. The blender should be checked by a qualified technician at the intervals specified in Section 11. All Bio-Med Devices blenders are tested for backflow at the factory. However, some level of backflow (10 ml./hr.) is acceptable per the ISO standard 11195. It is recommended that when not in use, either the blender supply gases should be detached from the blender (or turned off by installing on/off valves) or the blender bleed function should be left on, to prevent any chance of cross contamination. NOTES: The NEO2 BLEND with two flowmeters conforms to the model #2003 configuration with flow limited by the flowmeters. Refer to Addendum 2 in the beginning of this manual. This blender has been degreased for oxygen service prior to delivery. The upper flow limit is the total flow that the blender will pass, not the limit per port. This device has no latex content. Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.

2. EXPLANATION OF SYMBOLS Symbol

BS EN ISO 15223-1 Standard Ref

Definition / Explanation

MR Conditional- This device has been demonstrated to pose no known hazards in a specified MRI environment and with specified conditions of use.

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NA-ASTM F2503-05

MR Unsafe- This device is known to pose hazards in all MRI environments.

NA-ASTM F2503-05

NA

Follow Instructions for Use

5.4.4 Caution: Consult accompanying documents

i

Refer to manual for proper method of operation

Warning: Condensed water in air supply can cause malfunction of this device

Rx Only

5.4.3

NA-BMD

Warning: Do not obstruct alarm or bleed holes in the bottom of this device

NA-BMD

Product should be kept dry

5.3.4

Caution: Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner.

NA-per FDA guidance

5.1.3

Date of Manufacture

5.1.1

Manufacturer

SN

Serial Number

5.1.7

REF

Catalog Number

5.1.6

Authorized Representative in the European Community

The CE mark displayed on this product signifies that this device is in compliance with the European Medical Devices Regulation (2017/745). As a prerequisite for the CE mark, BioMed Devices operates under an ISO 13485 compliant quality system (covering the design and manufacture of medical devices). The four-digit code underlying the CE mark (2797) pertains to Bio-Med's Notified Body, the British Standards Institute, whose function is to investigate and attest to the validity of CE-mark claims.

Country of Manufacture

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5.1.2

Medical Device

Unique Device Identifier

Contains Hazardous Substances

3. SPECIFICATIONS Bio-Med Devices' line of blenders delivers accurate FIO2 mixtures from one to up to three outlet ports, allowing it to power three items at once. Several flow ranges are available. They can be used with ventilators, nasal cannulas, mask CPAP and resuscitation bags. The 0-50 LPM Blender is a perfect compromise between the High Flow and Low Flow blenders as it requires less of a bleed for accuracies below 6 LPM than the High Flow while allowing greater maximum flow than the Low Flow Blender. The Low Flow version of the blender provides flows from 3 to 30 LPM with no gas bleed. Bio-Med Devices also offers MR-conditional versions that are made entirely of non-magnetic materials. CAUTION: Do not use in an MRI room unless the blender has been built by Bio-Med Devices to be used for such an environment. This will be indicated by “MRI” on the blender front plate, and an MR-Conditional label on the case. Device-Specific Standards: Complies with ISO 11195. Oxygen % Range: 21 to 100% Oxygen % Accuracy: ±3% of full scale Supply Pressure: Both supplies within range of 30-75 PSI (207-517 kPa) and Air & oxygen must be within 10 PSI (69 kPa) of each other.* Do not use on a patient or with a ventilator outside of this range. *Blender performance with supply pressures below range (0-30 PSI / 0-207 kPa) cannot be predicted. Due to low output pressure, it will not be able to adequately drive a ventilator. Not for patient use. Blender performance with supply pressures above range (75-112.5 PSI / 517-775 kPa) with supplies balanced, available output flows, and oxygen percentages will remain consistent with specification. Output pressures will be proportionally higher and may damage the ventilator. Not for patient use. Maximum Flow: ≥120 LPM (≥50 LPM, 0-50 Flow blender; ≥30 LPM, Low Flow blender) @ 60% setting & 50 PSI (345 kPa) inlet pressures. Standard Flow Ranges: Refer to table in Section 4. Custom Configuration Flow Ranges: Refer to addendums and table in Section 4.

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Pressure Drop: <6 PSI (42 kPa) at 50 PSI (345 kPa) inlet pressure and 40 LPM flow (10 LPM, Low Flow blender). Low Supply Alarm: as described in Section 4. Alarm/Bypass Reset: when inlet gas pressure differential is ≥6 PSI (42 kPa). Alarm Intensity: 80 dB at 1 foot. Input fittings: Oxygen female DISS, Air male DISS (NIST available) Output Fitting(s): Male DISS, oxygen type. Dimensions:

Height 3 1/2" (8.9 cm) Width 2 1/4" (5.7 cm) Depth 2 7/8" (7.3 cm)

Weight: 2.35 lbs (1.07 kg) No electronics incorporated. Reverse Gas Flow: From either gas inlet to the other, complies with clause 9 of ISO 11195. Operating Temperature: 41° to 104° F (5° to 40° C) Ambient Humidity: 5 to 90% non-condensing

4. INTRODUCTION AND OPERATION The Bio-Med Air/Oxygen Blender is a precision proportioning device for mixing medical grade air and oxygen to any concentration from 21% to 100% oxygen and delivering it to a variety of respiratory care devices. The blender uses source air and oxygen at a pressure of 50 PSI (345 kPa) connected to two D.I.S.S. fittings on the bottom of the blender. Each fitting has a built-in 48 micron particulate filter. The gas source then passes through a duckbill check valve which prevents reverse gas flows from either source. The blender uses a double stage balancing system with the gas entering into the first stage to equalize the operating pressure of the gas sources before entering the proportioning stage. The gases then flow into the proportioning stage where they are mixed to the percentage dialed in on the front panel knob. This stage has a double-ended valve with valve seats on either end. Each one of these valve seats controls the passage of the air or oxygen to the outlet of the blender. Many different configurations of blenders and output ports are available. The model -5-

number can be found on the back of the blender. Use the front of the blender to identify which row to use in the table below to determine its flow range. The blender will be Low Flow, 0-50 LPM, High Flow or High/Low Flow. The flow limitations listed below apply, regardless of what is attached to the port. If the bleed is active, the “flows with bleed” applies to all output ports. Conversely, if the bleed is inactive, the “flows without bleed” applies to all ports. NOTE: The upper flow limit is the total flow that the blender will pass, not the limit per port. As an example, if 30 LPM is passing through any one port on a Low Flow blender, then no other port should be used as 30 LPM is the upper flow limit for this blender. The bleed referred to in the table and elsewhere in this manual is activated in one of three ways depending on what is on the right side of the blender. If there is a DISS fitting, attaching a device to this fitting will turn on the bleed1. If there is a knob, setting it to the “<” position will turn on the bleed (refer to Addendum 1). If there is a flowmeter on a switch mounted here, rotating it to its vertical position will turn on the bleed (refer to Addendum 2). If none of these options are available on the right side, then the bleed cannot be turned on and off. The bleed will either always or never be present. The latter is the case for the High Flow, which has no bleed available. 1

WARNING: Some special order blenders may not have a bleed when using the right DISS outlet. When this is the case, the flow specifications for without bleed apply.

FLOW TABLE Flow Range without Bleed 3-30 lpm

Flow Range with Bleed 0-30 lpm (3 lpm Bleed)

6-50 lpm

0-50 lpm (6 lpm Bleed)

High Flow

15-120 lpm (No Bleed)

N/A

High/Low Flow

15-120 lpm (No Bleed)

2-108 lpm (10-12 Bleed)

Model Low Flow Mid Flow (0-50 LPM)

NOTE: The NEO2 BLEND conforms to the Low Flow configuration with flow limited by the flowmeters. Refer to Addendum 2 in the beginning of this manual.

The blender has an audible alarm built in to detect if either of the gas sources changes by more than 20 PSI* (138 kPa) from the other. This will warn the user that they are running out of one of the gas sources or that there is a severe pressure drop in one source. If both gas sources drop or increase together such that a 20 PSI* (138 kPa) difference cannot be detected, then no alarm will sound. If the blender is connected but not being used and a 20 PSI* (138 kPa) difference in gas sources develops, the blender will not alarm. *(30 PSI [207 kPa] in the case of overseas devices and those manufactured for Draeger / Hill Rom / Air-Shields) The blender alarm/bypass function will provide > 90 LPM (the full 30 LPM, Low Flow Blender) upon the loss of air or oxygen, if the remaining gas is at 50 PSI (345 kPa).

5. SETTING UP THE BLENDER The Bio-Med Devices Blender can be either pole-, wall-, or rail-mounted for easy use for -6-

any desired application. The inlet fittings are located on the bottom of the blender and conform to Diameter Index Safety System (D.I.S.S.) so that air and oxygen connections cannot be reversed. Connect an air high pressure hose to the air fitting and an oxygen high pressure hose to the oxygen fitting on the bottom of the blender. Bio-Med Devices recommends an air inlet water trap be used between the air hose and inlet fitting to prevent moisture from entering the blender. The primary outlet (refer to Addendum 1) on the bottom of the standard high flow blender is appropriate for high flow situations, as with most ventilators requiring flows up to 120 LPM. Flows of less than 15 LPM (6 LPM, 0-50 LPM blender; 3 LPM, Low Flow blender) require the auxiliary right side outlet (knob or switching flowmeter). If both outlets are used simultaneously, neither one will deliver its maximum flow.

6. TESTING THE BLENDER The following checks should be performed before first placing the blender into service. Note: If the blender does not pass these checks, do not place the unit into service; call Bio-Med Devices Service Department at (203) 458-0202. First, connect the 50 PSI (345 kPa) air and oxygen sources to the appropriate fittings and set the blender to 60% (the alarm should not activate). Check to see that the oxygen concentration is actually 60% by using a calibrated oxygen monitor. Disconnect the oxygen source from the blender and listen for the audible alarm. Once it alarms, reconnect the oxygen to stop the alarm and verify the oxygen concentration again. Next, disconnect the air source from the blender and listen for the audible alarm. Once it alarms, reconnect the air and verify the oxygen concentration again.

7. USING THE BLENDER Connect the gas outlet of the blender either directly or via a high pressure hose to the ventilator or other equipment with which it is being used. Set the control on the front panel to the desired oxygen concentration. Turn on the 50 PSI (345 kPa) air and oxygen sources and set the controls on the ventilator or equipment being used. Use a calibrated oxygen analyzer to check the accuracy of the patient gas. When changing oxygen concentration, wait sixty seconds (equilibration time) before checking it against the analyzer. To use the standard high flow blender for low flow applications, connect a flowmeter to the secondary outlet (refer to Addendums 1 & 2 at the beginning of this manual), and set the concentration with the knob on the front panel. Turn on the source gases, set the flowmeter, and check the output with a calibrated oxygen monitor.

8. TROUBLE SHOOTING GUIDE PROBLEM

CAUSE OF PROBLEM

TO SOLVE PROBLEM

OXYGEN ANALYZER DOESN'T AGREE WITH SETTING OF BLENDER

ANALYZER OUT OF CALIBRATION

CALIBRATE OXYGEN ANALYZER

BLENDER OUT OF CALIBRATION

CALL BIO-MED SERVICE DEPARTMENT

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BLENDER ALARMING

THE ONLY TIME THE BLENDER IS ACCURATE IS WHEN THE SOURCE PRESSURES ARE EXACTLY THE SAME

DIRTY GAS SUPPLY

CALL BIO-MED SERVICE DEPARTMENT

BLEED ON BOTTOM OF BLENDER IS RESTRICTED

CALL BIO-MED SERVICE DEPARTMENT

AIR IS FLOWING INTO PIECE OF EQUIPMENT BEING USED AND DILUTING CONCENTRATION

CORRECT SITUATION BY STOPPING THE FLOW OF AIR

AIR AND OXYGEN SOURCE PRESSURES HAVE GREATER THAN 20 PSI* (138 kPa) DIFFERENTIAL

BRING THE SOURCE PRESSURES WITHIN THE 20 PSI* (138 kPa) RANGE

ALARM SYSTEM IS OUT OF CALIBRATION

CALL BIO-MED SERVICE DEPARTMENT

DIRTY GAS IS CONTAMINATING ALARM SYSTEM

CALL BIO-MED SERVICE DEPARTMENT

PRESSURE BALANCE CHAMBER NOT WORKING PROPERLY

CALL BIO-MED SERVICE DEPARTMENT

*(30 PSI [207 kPa] in the case of overseas devices and those manufactured for Draeger / Hill Rom / Air-Shields)

9. CLEANING INSTRUCTIONS Bio-Med Devices' line of blenders should be cleaned & disinfected by wiping the outside surfaces with alcohol (70% IPA) applied to a tissue or cloth. These blenders should never be sprayed with or immersed in any other liquid. Be sure not to allow ingress of any appreciable quantity of alcohol into any alarm or vent holes. Never insert anything into the holes in the alarm cover.

10. BLENDER WARRANTY The Bio-Med Devices, Inc. warranty lasts for one year from date of purchase. This warranty covers parts and labor. Shipping costs are covered up to six months from date of purchase. This warranty is limited to defects in parts and workmanship; Bio-Med Devices will not be held responsible for misuse or abuse of the product. All service must be done by Bio-Med Devices or an authorized service representative of Bio-Med Devices. Bio-Med Devices will not be held responsible for unauthorized service work on any blender.

11. SERVICE RECOMMENDATIONS Periodic preventive maintenance should be performed to ensure continued proper -8-

operation of the blender. The frequency of preventative maintenance is determined by many factors, some of which are: Frequency & length of use Quality of the compressed gas source(s) Environmental conditions Recommended Maintenance Schedule Interval

Recommended Procedures

Prior to each use

Performance test

Every year between PM’s

Calibration certification

Every 2 years

Major overhaul, cleaning and calibration Recommend return to factory for this service

12. TRAINING RECOMMENDATIONS Upon receipt of the BMD blender, the qualified medical professional should at a minimum read this manual in its entirety, and follow their own facility’s training guidelines for new equipment.

13. DEVICE LIFETIME & END-OF-LIFE DISPOSAL The device lifetime of this durable medical equipment is unlimited, if proper preventive maintenance is sustained, as per the Service Recommendations listed in this manual (and barring abusive usage conditions). In factory PM, all of the components subject to normal wear are replaced. If the device ceases to function in specification, it should be returned to the factory for evaluation. Significant adverse usage events (e.g., unreasonable impact) might render the device beyond justifiable repair, for safety or financial reasons. Cease to reuse this device if out-of-spec operation is detected, or if physical signs of serious damage are noted (e.g., a skewed control knob, or fluid ingress). To decommission the BMD Blender, the user may send it back to Bio-Med Devices for proper disposal and recycling of all applicable components. If this is not practical, the user may disassemble the device and recycle components using local recycling resources. It is recommended to separate out the brass, aluminum, and other metals for recycling. Elastomers should be discarded. There are no internal batteries or electronics. Please consider these potential hazards before attempting disassembly of the BMD Blender: -Do not attempt dis-assembly with gas sources attached. -Beware sharp corners of metal parts, which could cut one’s hands.

This device and its packaging contain no hazardous materials. No special precautions need to be taken when disposing of the device and/or its packaging.

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14. MATERIALS CONTENT Individual internal components of this device contain the following IARC group 1 material of note, with content % per sub-part (not of the entire device) greater than 0.1% by weight: Lead (only alloyed with copper, and always <4% by weight content of each individual copper alloy sub-part) No special precautions are necessary on the part of the user (or patient). This includes use for potentially vulnerable populations such as children and pregnant or breastfeeding women, to whom accrue no known residual risks of the presence of these copper alloys in respiratory equipment. Such copper alloys have been a standard construction material in respiratory devices for decades, and have a specific exemption under the RoHS directive.

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APPENDIX A

Authorized Representative in the European Community: Bio-Med Devices’ Official Agent in Europe is: Medicare Uitgeest BV Westerwerf 10 1911JA Uitgeest The Netherlands NL Telephone: +31 251 316358

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APPENDIX B BMD Air/Oxygen Blender MR Information Non-clinical testing has demonstrated that the BMD MR-version Air / Oxygen Blenders (only the blenders built specifically for MR usage, with an “M” suffix on the model #, and an “MRI” screened on the front plate) are MR Conditional. They can be scanned safely under the following conditions: •

Static magnetic field of 3-Tesla

•

Spatial gradient field of 472-Gauss/cm or less

•

Maximum MR system reported, whole body averaged specific absorption rate (SAR) of 2-W/kg for 15 minutes of scanning

•

MR image quality may be compromised if the area of interest is in the same area or relatively close to the position of the device. Therefore, it may be necessary to optimize MR imaging parameters for the presence of this device.

•

Additional requirements:

The Blender must be used with the BMD MR-conditional stand, and the stand’s wheels that have integral wheel locks must be locked. Do not place the Blender & stand closer than one foot away from the MR bore (do not place the Blender inside the MR bore). If using supply gas cylinders and regulators, use only MR-conditional aluminum gas cylinders and regulators (observe manufacturer’s published MR-conditional requirements).

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APPENDIX C UDI NUMBERS 2000K 2000KM 2001 2001B 2001F 2001FB 2001FEU 2001FEUB 2001K 2001KB 2001M 2001MB 2001N 2001T

813841020072 813841020089 813841020034 813841021062 813841020096 813841021079 813841020102 813841021253 813841020119 813841021086 813841020126 813841021093 813841020966 813841020485

2002 2002F60A 2002F70 2002F70A 2002F70B 2002F70D 2002F70X 2002FP70 2002K 2002K2 2002L 2002M

813841020041 813841020508 813841020133 813841020515 813841021109 813841020140 813841020461 813841020157 813841020164 813841020171 813841022212 813841020188

2003 2003AJ1 2003AJ2 2003AJ3 2003AS 2003AS1 2003B 2003C 2003D 2003DA 2003EF15B 2003EF1B 2003EFB 2003F 2003FF 2003FF1 2003FF15 2003FF15B 2003FF1B 2003FF2B

813841020058 813841020522 813841020539 813841020546 813841021048 813841021055 813841021116 813841020553 813841020560 813841020577 813841021123 813841021130 813841021147 813841020195 813841020201 813841020218 813841020225 813841021154 813841021161 813841021178

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2003FFA 2003FFAB 2003FFB 2003FFE1 2003FFE5 2003FFEA 2003FFEU 2003FFEUC 2003FFFP 2003FFG 2003FFH 2003FFJ 2003FFK 2003FFN 2003FFQ 2003FFR 2003FL 2003FLA 2003FLB 2003FLEU 2003FLEUX 2003FP 2003FQ 2003GE 2003H 2003I 2003IB1 2003IB2 2003K 2003KA 2003KB 2003KC 2003KJ 2003M 2003MB 2003N 2003P 2003Q 2003T 2003U

813841020232 813841021185 813841021192 813841020249 813841020256 813841020263 813841020270 813841020584 813841020287 813841020591 813841020294 813841020300 813841020607 813841020317 813841020324 813841020935 813841020331 813841020348 813841021208 813841020355 813841020478 813841022199 813841022205 813841020010 813841020430 813841020614 813841020447 813841020454 813841020362 813841020638 813841021215 813841020379 813841020386 813841020393 813841021222 813841020973 813841021260 813841021277 813841020492 813841021307

2004 2004B 2004F7015 2004F7015A 2004F7015EU 2004F7015X 2004I 2004M 2004MB

813841020065 813841021239 813841020409 813841020416 813841020942 813841020959 813841020645 813841020423 813841021246

21471

813841020928

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