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Coulmed

FDA UDI

Class I (US FDA UDI)

by Coulmed Products Group Llc

Identity

Trade Name
Coulmed FDA UDI
Generic Name
Non-wearable adult urine collection bag, open-ended FDA UDI
Device Name
Urology Drain Collection Bag: 5-Gallon Capacity, Built in Handles, Connection tube/hose included FDA UDI
Model / Reference
A5010 FDA UDI
Description
Urology Drain Collection Bag: 5-Gallon Capacity, Built in Handles, Connection tube/hose included FDA UDI

Identifiers

Catalog Number
A5010 FDA UDI
Primary DI / UDI-DI
10810087350489 FDA UDI
FDA Product Code
NNW FDA UDI
GMDN Term
Non-wearable adult urine collection bag, open-ended FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Coulmed by Coulmed Products Group Llc — Class I — 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 60dfe98e-8922-499b-9549-ffa963157e77 34 fields · synced May 30, 2026