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Mabis Dmi

FDA UDI

Class II (US FDA UDI)

by Dms Holdings, Inc.,

Identity

Trade Name
MABIS DMI FDA UDI
Generic Name
Adhesive paediatric urine collection bag, open-ended FDA UDI
Device Name
U-BAG STERILE STANDARD ADHESIVE PEDIATRIC FDA UDI
Model / Reference
D 7511 FDA UDI
Description
U-BAG STERILE STANDARD ADHESIVE PEDIATRIC FDA UDI

Identifiers

Catalog Number
D 7511 FDA UDI
Primary DI / UDI-DI
10767056075112 FDA UDI
FDA Product Code
FOC FDA UDI
GMDN Term
Adhesive paediatric urine collection bag, open-ended FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5250 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

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

Mabis Dmi by Dms Holdings, Inc., — 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
Dms Holdings, Inc.,

Sources (1)

  • FDA UDI e6a6ae9b-1db0-492e-9ebf-ff5003a155f1 35 fields · synced May 31, 2026