IMUFLEX WB-SP BLOOD BAG SYSTEM WITH INTEGRAL WHOLE BLOOD LEUKOCYTE REDUCTION FILTER (SAVING PLATELETS) WITH DIVERSION BLOOD SAMPLING ARM (anticoagulant citrate phosphate dextrose- cpd solution
imuflex wb-sp blood bag system with integral whole blood leukocyte reduction filter (saving platelets) with diversion blood sampling arm by
Drug Labeling and Warnings
imuflex wb-sp blood bag system with integral whole blood leukocyte reduction filter (saving platelets) with diversion blood sampling arm by is a Prescription medication manufactured, distributed, or labeled by Terumo Corporation, Terumo Corp. - Fujinomiya Factory. Drug facts, warnings, and ingredients follow.
Drug Details [pdf]
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SPL UNCLASSIFIED SECTION
NDC: 53877-010-01
CPD SOLUTION
For the collection of 500 mL of Whole BloodFULL PRESCRIBING INFORMATION
*Sections or subsections omitted from the Full Prescribing Information are not listed [includes sections 4, 6, 7, 8, 9, 10, 12, 13, 14, 15 and 17]. -
1. INDICATIONS AND USAGE
1.1. Read these instructions carefully before use.
1.2. Rx ONLY.
1.3. Intended for the collection, processing and preservation of Whole Blood. Not intended for direct intravenous infusion.
1.4. For the collection of 500 mL ±10% Whole Blood.
1.5. Integral Diversion Blood Sampling Arm is intended to divert and obtain donor samples for laboratory testing prior to collection of the Whole Blood unit.
1.6. Integral filter unit intended for leukocyte reduction of Whole Blood up to 8 hours after blood collection when Whole Blood is stored at ambient temperature.
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2. DOSAGE AND ADMINISTRATION
2.1. Prepare the blood bag following your institution's standard operating procedures.
2.2.1. Materials Needed : Evacuated blood collection tubes (glass or plastic)
2.2. Make a loose knot in the donor tubing below the "Y" and CLIKTIP® (inline closure device) unless alternate methods are used to seal the tubing at the end of collection.
2.3. Temporarily clamp donor tubing between the phlebotomy needle and the "Y".
2.4. Suspend the collection bag as far as possible below the donor's arm.
2.5. Apply blood pressure cuff or tourniquet to donor's arm. Disinfect site of phlebotomy. If blood pressure cuff is used, inflate to approximately 60 mmHg.
2.6. Remove the needle cover and perform phlebotomy. Remove the temporary clamp on the donor tubing to permit blood flow into the Diversion Blood Sampling Arm pouch.
2.6.1. CAUTION: Do not touch the needle after removing the needle cover.
2.7. Secure the needle safety device in place following the device instructions provided on the reverse side.
2.8. Secure donor tubing to donor's arm.
2.9. Position the diversion pouch with the notches up and the Tube Holder/Luer Adapter assembly down. When the level of blood in the pouch is approximately in line with the notches, the diversion pouch is full. (Fig. 2a)
2.9.1. NOTE: The approximate fill volume of the pouch at the notches is 35 mL.
2.10. Permanently seal the tubing between the "Y" and the diversion pouch to maintain a closed system using an aluminum clip or a tube sealer approved for use with tubing connected to a donor (Fig. 2b).
2.10.1. CAUTION: Do not use a dielectric tube sealer to seal the tubing while the needle is connected to the donor's body unless it is approved for such a purpose.
2.11. To initiate blood flow into the collection bag, break the CLIKTIP between the "Y" and the collection bag.
2.12. To avoid clot formation, collect samples as soon as possible from the diversion pouch as follows (Fig. 2b).
2.12.1. CAUTION: Do not collect donor test samples until the tubing between the "Y" and the diversion pouch is permanently sealed.
2.12.2. Break the CLIKTIP in the tubing below the pouch to open the pathway for sampling. (Fig. 2b)
2.12.3. Position the diversion pouch with the notches up and the Tube Holder/Luer Adapter assembly downward. Assure that any air in the pouch is at the top and will not enter the blood collection tubes.
2.12.4. Open the Tube Holder lid and insert blood collection tube firmly into the tube holder; when full, remove sample tube from holder. Repeat to collect additional samples.
2.12.5. NOTE: The pouch may be removed after the donor test samples are collected. A second seal must be made between the diversion pouch and the permanent seal prior to removing the pouch.
2.13. Mix blood with anticoagulant in the collection bag and continue to mix at several intervals during collection and immediately after collection. If using an automated mixer, follow manufacturer's instructions.
2.14. Collect labeled volume of blood 500 mL ±10%.
2.15. When the desired amount of blood has been collected, seal the tubing or tighten the loose knot (white knot) prepared in Step 2.2. Make a second seal between the first seal or knot and the "Y". Various methods may be used to seal tubing.
2.16. Release pressure on the donor's arm and remove the needle into the needle safety device following the device instructions provided on the reverse side. Sever the donor tubing between the two seals previously made below the CLIKTIP and "Y".
2.16.1. CAUTION: Discard the Diversion Blood Sampling Arm and phlebotomy needle/donor tubing according to institutional standard operating procedures.
2.17. Seal and remove donor tubing from collection bag or strip donor tubing as follows:
2.17.1. To obtain a quality control prefiltration sample, strip blood from donor tubing into collection bag, mix well, and allow tubing to refill; repeat once. To prevent the blood from clotting in the tubing, work quickly as possible. Leave an adequate length of tubing containing the well-mixed anticoagulated whole blood attached to the collection bag.
2.17.2. Or, to maximize collection recovery, strip the tubing, mix well and seal tubing close to the collection bag without refilling. To prevent the blood from clotting in the tubing, work quickly as possible. Remove tubing from collection bag.
2.18. The blood filtration is executed according to the following operation. (see Fig.3 and Fig.4)
2.18.1. NOTE: Wait 1 hour after collection before filtering. Filtration can be accomplished when blood is stored at room temperature for up to eight hours after collection.
2.18.2. NOTE: The band guides used to bundle the coiled tubing to prevent entanglement during shipping should be removed prior to filtration (not depicted).
2.19. Mix the unfiltered whole blood unit by inverting the collection bag #1 (pre-filter bag) several times.
2.20. Hang the collection bag #1, and extend the filtration set to 85 ± 2.5 cm or 33.5 ± 1 inch. Verify that the filter is vertical and ensure all tubing is freely suspended. Position and support bags #2 on a flat surface (Fig. 4).
2.20.1. NOTE: This distance is measured from the outlet of the collection bag to the position of the supported bags as indicated in Fig. 4.
2.20.2. NOTE: Verify tubing has been removed from the tube guides and extends freely.
2.21. Break the CLIKTIP at the outlet of the collection bag #1, and start filtration.
2.21.1. CAUTION: Do not squeeze the collection bag during filtration.
2.21.2. CAUTION: Do not squeeze or apply pressure on the filter while it is attached to the bag containing the filtered blood.
2.21.3. CAUTION: If for any reason whole blood passes through the one-way valve, stop filtration immediately and consider the product as non-leukocyte reduced.
2.22. Filtration ends when the collection bag is empty or blood flow has stopped. Close the WHITE clamp above the filter.
2.23. Expel air through the bypass line and back into the empty collection bag #1 by holding the primary bag #2 upright so that the air will be closest to the ports. Gently squeeze the primary bag containing the leukoreduced whole blood until filtered blood reaches the "Y" below the filter. To ensure ease of air removal ensure primary bag #2 is below the filter outlet.
2.24. Open the WHITE clamp.
2.25. Recovery of filtered Whole Blood is complete when the collection bag and the inlet side of the filter have drained or blood flow has stopped. Close the WHITE clamp.
2.26. Seal the tubing as close as possible to the "Y" below the filter and properly dispose of the filter and collection bag #1.
2.27. Strip the post filter tubing into the primary bag #2, mix well, and allow tubing to refill; repeat once. Make an appropriate number of segments of anticoagulated blood for testing by sealing on or near the X marks. Leave segments attached to the filtered whole blood unit.
2.28. Mix CPD solution and whole blood thoroughly.
2.28.1. NOTE: Whole blood in CPD may be stored for up to 21 days at 1-6°C.
- 3. DOSAGE FORMS AND STRENGTHS
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5. WARNINGS AND PRECAUTIONS
5.1. Rx ONLY.
5.2. Do not use unless solutions are clear and free from particulates.
5.3. Always inspect the blood bag set for leaks before use.
5.4. Avoid excessive heat and direct sunlight. Protect from freezing.
5.5. Recommended storage conditions: Room Temperature (15-30°C/59-86°F).
5.6. It is normal to have condensation in the aluminum foil pack. If the amount of moisture is greater than expected, check for leaks from the fluid-filled components of the blood bag set.
5.7. Use aseptic techniques.
5.8. Do not use a dielectric tube sealer to seal the tubing while the needle is connected to the donor's body unless it is approved for such a purpose.
5.9. Do not touch needle after removing the needle cover.
5.10. Do not collect donor test samples until the tubing between the "Y" and the diversion pouch is permanently sealed.
5.11. Discard the Diversion Blood Sampling Arm and phlebotomy needle/donor tubing according to institutional standard operating procedures.
5.12. Each aluminum foil pack contains a sachet that absorbs oxygen and generates heat on contact with air. The sachet should be handled with caution.
5.12.1. Do not open the oxygen absorber sachet.
5.12.2. Dispose of the aluminum foil pack with the oxygen absorber sachet in the pack.
5.12.3. Do not dispose of the aluminum foil pack containing the oxygen absorber sachet together with waste containing volatile or flammable material.
5.13. Due to possible exposure to infectious agents in the handling of blood, take adequate precautions at all times to prevent exposure to and transmission of such agents. Follow your institution's standard operating procedures.
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11. DESCRIPTION / PRODUCT SPECIFICATIONS
11.1. This blood bag system includes a 16 gauge × 1 1/2 inch (1.60 × 38 mm) needle with needle cover and a 500mL collection bag containing 70mL Citrate Phosphate Dextrose (CPD) anticoagulant. The Double blood bag set has one integrally attached empty primary bag.
11.2. Blood bag collection set is the collection set with an Integral Diversion Blood Sampling Arm for obtaining donor samples prior to collection of the Whole Blood Unit.
11.3. Blood bag collection set is also included a DonorCare® Needle Guard pre-attached to the donor tubing. DonorCare Needle Guard device instructions are provided on the reverse side.
11.4. The blood bag collection set is made of PVC (polyvinyl chloride with DEHP plasticizer).
11.5. The blood bag has no components made of natural rubber latex.
11.6. Tubing internal diameter (ID) nominal 3.0 mm.
11.7. Tubing outer diameter (OD) nominal 4.4 mm.
11.8. Tubing line maximum 16 segments available.
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16. HOW SUPPLIED/STORAGE AND HANDLING
16.1. Single use only.
16.2. Sterile and non-pyrogenic fluid path. Sterilized by steam. Opacity of the blood bag system may be observed. This is due to moisture absorption during the sterilization process. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually.
16.3. Use immediately after opening aluminum foil pack.
16.4. A Safety Data Sheet (SDS) is not required for this product.
16.5. Recommended storage conditions: Room Temperature (15-30°C/59-86°F).
16.6. Avoid excessive heat and direct sunlight. Protect from freezing.
16.7. Each aluminum foil pack contains a sachet that absorbs oxygen and generates heat on contact with air. The sachet should be handled with caution.
16.8. For the Double blood bag set, Code BB*LCD506A6 is supplied. 10/case.
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SPL UNCLASSIFIED SECTION
MANUFACTURED BY:
TERUMO CORPORATION
44-1, 2-CHOME, HATAGAYA, SHIBUYA-KU,
TOKYO 151-0072, JAPAN MADE IN JAPAN® : Registered Trademark
© TERUMO CORPORATION December, 2018TERUMO is a trademark of TERUMO CORPORATION.
DonorCare is a registered trademark of Noble House Group Pty. Ltd. CORPORATION.
Issued 2018-12
N-LCD506A6 2 -
PROCEDURE FOR USE OF DonorCare® Needle Guard
This device is for use by trained individuals.
Intended Use
The DonorCare® Needle Guard is incorporated onto the donor tubing to shield the needle immediately after withdrawal from the donor.
Single Use Only.
Preparation
1. Move the DonorCare on the tubing ensuring that it slides easily and the arrow is pointing toward the needle hub.
2. Ensure that the three lock points on the DonorCare are locked closed.
Whole Blood Collection
3. Perform the phlebotomy as per your institution's standard operating procedures.
4. Slide the DonorCare over the needle hub so that it covers approximately one half to two thirds of the needle hub.
5. Stabilize the DonorCare to the arm by placing a piece of tape over the front end so that the tape does not extend over the front of the DonorCare.
Withdrawal of Needle
Important
The DonorCare must be held stationary while the needle is withdrawn into it.
Caution
The needle must be fully shielded by DonorCare to prevent accidental injury.
6. Hold gauze over the venipuncture site with finger tips without exerting pressure. Hold the sides of the DonorCare near the front with the index finger and thumb of the same hand.
7. With the other hand, hold the donor tubing close behind the DonorCare.
Note: A hemostat may be placed on the tubing behind the DonorCare when the blood collection is complete.
This will help to prevent blood drops from forming.
8. Pull tubing smoothly and swiftly with one motion until the needle is locked in place inside the DonorCare.
9. Confirm that the needle is locked by:
a. Listening for two 'clicks' as the needle is drawn into DonorCare.
b. If the clicks are not heard as the needle is drawn into the DonorCare, continue to pull firmly on the tubing to assure needle is fully withdrawn into DonorCare.
10. Visually check that the needle is fully shielded by DonorCare before removing from the donor's arm.
11. Remove the tape from the DonorCare and arm.
12. Apply pressure to the gauze covering the venipuncture site.
Warning
Do not place fingers at the opening of DonorCare after removal from the donor's arm.
Difficult Phlebotomy (Examples may include: Slow blood flow, deep or fine vein, steep angle)
It may be necessary to delay placing the DonorCare over the needle hub until the end of the blood collection. In such situations:
Leave the DonorCare on the tubing behind the needle hub. At the end of the blood collection carefully remove the tape from the needle hub and slide the DonorCare over the hub so that it covers approximately one half to two thirds of the needle hub. Withdraw the needle into the DonorCare as stated in steps 6. through 12. above.
Rx ONLY
DonorCare is manufactured by ITL Corporation, Melbourne, Australia.
DonorCare is a registered trademark of Noble House Group Pty. Ltd. CORPORATION.
TERUMO CORPORATION
44-1, 2-CHOME, HATAGAYA, SHIBUYA-KU,
TOKYO 151-0072, JAPAN© TERUMO CORPORATION December, 2018
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PRINCIPAL DISPLAY PANEL - 70 mL Bag Pouch Carton
THIS WAY UP
FRAGILE
KEEP AWAY
FROM SUNLIGHT
KEEP DRY
STACKING LIMIT
BY NUMBERRx Only
IMUFLEX®
WB-SPRecommended Storage : Room Temperature
(15-30°C/59-86°F)
Avoid excessive heat, Protect from freezing.
Sterile, Non-pyrogenic fluid path.
Do not use unless anticoagulant is clear.
Use immediately after opening aluminum foil pack.
See Instructions For Use.10
ContentsTERUMO
CPD SOLUTION
FOR COLLECTION OF 500mL OF BLOODEach unit consists of a collection bag containing 70mL of
Anticoagulant CPD solution.Each 70mL Anticoagulant CPD solution USP contains
1.79g Dextrose (monohydrate) USP, 1.84g Sodium Citrate
(dihydrate) USP, 209mg Citric Acid (anhydrous) USP,
156mg Monobasic Sodium Phosphate (monohydrate) USP.
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INGREDIENTS AND APPEARANCE
IMUFLEX WB-SP BLOOD BAG SYSTEM WITH INTEGRAL WHOLE BLOOD LEUKOCYTE REDUCTION FILTER (SAVING PLATELETS) WITH DIVERSION BLOOD SAMPLING ARM
anticoagulant citrate phosphate dextrose (cpd) solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 53877-010 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dextrose Monohydrate (UNII: LX22YL083G) (Anhydrous Dextrose - UNII:5SL0G7R0OK) Dextrose Monohydrate 1.79 g in 70 mL Trisodium Citrate Dihydrate (UNII: B22547B95K) (Anhydrous Citric Acid - UNII:XF417D3PSL) Anhydrous Citric Acid 1.84 g in 70 mL Anhydrous Citric Acid (UNII: XF417D3PSL) (Anhydrous Citric Acid - UNII:XF417D3PSL) Anhydrous Citric Acid 209 mg in 70 mL Sodium Phosphate, Monobasic, Unspecified Form (UNII: 3980JIH2SW) (Phosphate Ion - UNII:NK08V8K8HR, Sodium Cation - UNII:LYR4M0NH37) Sodium Phosphate, Monobasic, Unspecified Form 156 mg in 70 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 53877-010-01 10 in 1 CARTON 1 1 in 1 POUCH 1 70 mL in 1 BAG; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA BN880217 02/11/2019 Labeler - Terumo Corporation (690543319) Establishment Name Address ID/FEI Business Operations Terumo Corp. - Fujinomiya Factory 695214015 MANUFACTURE(53877-010) , STERILIZE(53877-010) , ANALYSIS(53877-010) , LABEL(53877-010)
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