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Hopkins Medical Products®

FDA UDI

Class II (US FDA UDI)

by Hopkins Uniform Company

Identity

Trade Name
Hopkins Medical Products® FDA UDI
Generic Name
Wearable adult urine collection bag, open-ended FDA UDI
Device Name
Bedside Urinary Bag 2000cc FDA UDI
Model / Reference
34268 FDA UDI
Description
Bedside Urinary Bag 2000cc FDA UDI

Identifiers

Catalog Number
34268 FDA UDI
Primary DI / UDI-DI
00817643020254 FDA UDI
FDA Product Code
KNX FDA UDI
GMDN Term
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

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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wearable adult urine collection bag, open-ended

Hopkins Medical Products® by Hopkins Uniform Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hopkins Uniform Company

Sources (1)

  • FDA UDI 6b2bbb56-f9dc-4192-bd9f-3451e0168dc8 35 fields · synced May 30, 2026