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Transfer Pack

FDA UDI

Class II (US FDA UDI)

by Fenwal, Inc.

Identity

Trade Name
Transfer Pack FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Transfer Pack Container 600 mL with Male Luer Adapter. Sterile Fluid Path FDA UDI
Model / Reference
4R2024 FDA UDI
Description
Transfer Pack Container 600 mL with Male Luer Adapter. Sterile Fluid Path FDA UDI

Identifiers

Catalog Number
4R2024 FDA UDI
Primary DI / UDI-DI
10811137010551 FDA UDI
FDA Product Code
KSR FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9100 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Transfer Pack by Fenwal, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fenwal, Inc.

Sources (1)

  • FDA UDI b00887a9-1282-4236-bd45-0474734dbfc7 36 fields · synced May 31, 2026