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Asp Medical

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
ASP MEDICAL FDA UDI
Generic Name
Non-wearable adult urine collection bag, open-ended FDA UDI
Device Name
URINE COLLECTION BAG, 4L, LATEX FREE, 1/EA FDA UDI
Model / Reference
UBT440 FDA UDI
Description
URINE COLLECTION BAG, 4L, LATEX FREE, 1/EA FDA UDI

Identifiers

Primary DI / UDI-DI
00840216101609 FDA UDI
FDA Product Code
NNZ 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Asp Medical by Asp Global, 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

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI e264c822-7510-4a40-a139-2647544bbe5d 33 fields · synced May 31, 2026