STERILE CORD BLOOD COLLECTION UNIT - cord blood collection unit solution 
Medsep Corporation

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Sterile Cord Blood Collection Unit
Code 791-08

ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION (CPD)

Sterile, non-pyrogenic fluid path. Sterilized by steam.

Rx only.

This product is free of natural rubber latex.

INDICATIONS AND USAGE

For collection of up to 210 ml of umbilical cord blood. Use aseptic technique.

Sterile Exterior

Contents inside overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged; visual inspection to confirm the integrity of overwrap pouch should be performed.

WARNINGS

Do not irradiate collected cord blood or components.

Making multiple punctures of the umbilical cord to increase collection volume may increase the risk of contamination.

GENERAL PRECAUTIONS

Do not use if the package is damaged or seal is incomplete. Use only if solution is clear.

Sealing should be done in a manner that avoids fluid splatter.

Always dispose of blood-contaminated products in a manner consistent with established BIOHAZARD safety procedures.

HOW SUPPLIED

The Collection Unit inside the overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged.

INFORMATION FOR PATIENTS

Medsep Corporation, A Subsidiary of Pall Corp., Covina, CA 91722, USA

Visit us at www.pall.com/medical

For Pall customer service, call: 1.800.645.6578

DonorCare is a registered trademark of ITL Corporation, Canberra, Australia. Produced under license from ThermoGenesis Corp.

Instructions for Use

1. Ensure DonorCare® Needle Guard (DCNG) is positioned on the tubing between the needle hub and Pinch Clamp. Engage Pinch Clamp. Ensure tethered cap is placed securely on the air vent.

2. Using aseptic technique, insert needle into umbilical vein, disengage Pinch Clamp to collect cord blood, mixing frequently, according to standard procedures.

3. Upon completion of collection, engage Pinch Clamp then withdraw needle from umbilical vein. Slide the DCNG midway over the needle hub. While holding the sides of DCNG near front, grasp tubing and pull smoothly, pulling needle into the DCNG until it locks into place. Confirm that needle is locked by listening for the second click as the needle is drawn into the DCNG. Ensure that tubing cannot be pulled through DCNG.

4. Place the bag on a work surface. While holding the tubing above the bag, open the tethered cap on the air vent. Allow the blood to drain from the tubing into the bag.

5. When the tubing has been drained, hold tubing vertical and seal tubing directly below the Y-piece with air vent.

6. Detach and discard needle, DCNG, Pinch Clamp, Air Vent and tubing according to standard procedures.

7. Determine amount of anticoagulated blood collected. If required, add sedimenting agent to CPD anticoagulated blood through Sample Port using a syringe according to standard procedures.

8. Mix well. Take care to strip and mix any blood in tubing.

9. Load bag into centrifuge cup. It is suggested that a means of support is used to prevent bag from collapsing and to reduce wrinkles.

10. Centrifuge according to standard procedures to obtain mononuclear cell-rich plasma.

Cord Blood Collection Unit

BAG LABEL

Collection Bag Label

Collection Bag Label

HPC, Cord Blood

ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION

35 ml Anticoagulant Citrate Phosphate Dextrose Solution for collection of up to 210 ml of umbilical cord blood. Each 35 ml of CPD solution contains 0.921 g sodium citrate (dihydrate), USP; 0.893 g dextrose (monohydrate), USP; 0.114 g citric acid (monohydrate), USP; and 0.078 g monobasic sodium phosphate (monohydrate), USP. Use only if solution is clear.

Warning: This product may transmit infectious agents. Sterile, nonpyrogenic fluid path. Do not irradiate. Rx only.

Code 791-08

Issued August 2010, 147791082

STERILE CORD BLOOD COLLECTION UNIT 
cord blood collection unit solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:62646-791
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM CITRATE (UNII: 1Q73Q2JULR) (CITRIC ACID - UNII:2968PHW8QP) SODIUM CITRATE0.921 g  in 35 mL
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (DEXTROSE - UNII:IY9XDZ35W2) DEXTROSE MONOHYDRATE0.893 g  in 35 mL
CITRIC ACID (UNII: 2968PHW8QP) (CITRIC ACID - UNII:2968PHW8QP) CITRIC ACID0.114 g  in 35 mL
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHORIC ACID - UNII:E4GA8884NN) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE0.078 g  in 35 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62646-791-0835 mL in 1 BAG
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA80022203/16/2011
Labeler - Medsep Corporation (928224765)
Registrant - Medsep Corporation (928224765)
Establishment
NameAddressID/FEIBusiness Operations
Medsep Corporation928224765manufacture, relabel, repack

Revised: 3/2011
Document Id: 1b36f09f-c2cc-429a-859e-a673fc50ad1b
Set id: 836cb352-d1ea-455c-ba6f-ea9aa0c973fe
Version: 3
Effective Time: 20110309
 
Medsep Corporation