← Back to catalogue

Leukocyte SC RC

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
Leukocyte SC RC FDA UDI
Generic Name
Blood transfusion filter FDA UDI
Device Name
Leukocyte Reduction Filter System for Red Blood Cells with BPF4 High Efficiency Filter, 16-Segment Tubing, Storage Bag and Sample Pouch FDA UDI
Model / Reference
430-40 FDA UDI
Description
Leukocyte Reduction Filter System for Red Blood Cells with BPF4 High Efficiency Filter, 16-Segment Tubing, Storage Bag and Sample Pouch FDA UDI

Identifiers

Primary DI / UDI-DI
20887691308745 FDA UDI
FDA Product Code
CAK FDA UDI
GMDN Term
Blood transfusion filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfusion filter

Leukocyte SC RC by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfusion filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 56aa0691-89f3-4062-b4f6-219706e4034b 35 fields · synced Jun 8, 2026