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Brodmerkel

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Brodmerkel FDA UDI
Generic Name
Colonic decompression tube FDA UDI
Device Name
Brodmerkel Colon Decompression Set FDA UDI
Model / Reference
G22214 FDA UDI
Description
Brodmerkel Colon Decompression Set FDA UDI

Identifiers

Catalog Number
CDSB-10 FDA UDI
Primary DI / UDI-DI
00827002222144 FDA UDI
FDA Product Code
FEG FDA UDI
GMDN Term
Colonic decompression tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Brodmerkel by Cook Incorporated — 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
Cook Incorporated

Sources (1)

  • FDA UDI 81655188-ab86-46aa-9771-30d18a7a016a 37 fields · synced Jun 8, 2026