← Back to catalogue

Fenwal CompoSampler

FDA UDI

Class I (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
Fenwal CompoSampler FDA UDI
Generic Name
Blood collection tube holder, single-use FDA UDI
Device Name
Fenwal CompoSampler FDA UDI
Model / Reference
6R4011 FDA UDI
Description
Fenwal CompoSampler FDA UDI

Identifiers

Catalog Number
6R4011 FDA UDI
Primary DI / UDI-DI
04086000903141 FDA UDI
FDA Product Code
KST FDA UDI
GMDN Term
Blood collection tube holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.9125 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

Yes

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 collection tube holder, single-use

Fenwal CompoSampler by Fresenius Kabi — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection tube holder, single-use.

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

Manufacturer
Fresenius Kabi

Sources (1)

  • FDA UDI eea4e94c-98a3-407a-91bd-e24e370a22dc 35 fields · synced Jun 1, 2026