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Global Healthcare

FDA UDI

Class II (US FDA UDI)

by Ghc Healthcare, Inc.

Identity

Trade Name
GLOBAL HEALTHCARE FDA UDI
Generic Name
Non-wearable adult urine collection bag, open-ended FDA UDI
Device Name
URINE BAG, 2,000ML, RECTANGULAR SHAPE, ANTI REFLUX VALVE, HANGER, SAMPLING PORT, FLUID PATHWAY STERILE. FDA UDI
Model / Reference
UB-RC FDA UDI
Description
URINE BAG, 2,000ML, RECTANGULAR SHAPE, ANTI REFLUX VALVE, HANGER, SAMPLING PORT, FLUID PATHWAY STERILE. FDA UDI

Identifiers

Primary DI / UDI-DI
00872237004270 FDA UDI
FDA Product Code
KNX FDA UDI
GMDN Term
Non-wearable adult urine collection bag, open-ended FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5250 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

Yes

FDA UDI

Category: Non-wearable adult urine collection bag, open-ended

Global Healthcare by Ghc Healthcare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-wearable adult urine collection bag, open-ended.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7be036db-968f-4d59-92bb-5b559effc308 33 fields · synced May 31, 2026