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Fenwal Product Sample Pack

FDA UDI

Class II (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
Fenwal Product Sample Pack FDA UDI
Generic Name
Blood transfer set FDA UDI
Device Name
For Sampling of Collected Blood and Blood Components. For Laboratory Testing Only. Sterile Fluid Path. FDA UDI
Model / Reference
4R2335H FDA UDI
Description
For Sampling of Collected Blood and Blood Components. For Laboratory Testing Only. Sterile Fluid Path. FDA UDI

Identifiers

Catalog Number
4R2335H FDA UDI
Primary DI / UDI-DI
14086000101421 FDA UDI
FDA Product Code
KSR FDA UDI
GMDN Term
Blood transfer set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9100 FDA UDI
Commercial Distribution
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood transfer set

Fenwal Product Sample Pack by Fresenius Kabi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fresenius Kabi

Sources (1)

  • FDA UDI 65c4d792-d601-4b17-970e-994c760c25ab 36 fields · synced Jun 8, 2026