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Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Urethral catheterization support kit, urinary drainage FDA UDI
Device Name
BAG,DRAINAGE,UROLOGY,2000ML,ANTIREFLUX,E FDA UDI
Model / Reference
URO53211 FDA UDI
Description
BAG,DRAINAGE,UROLOGY,2000ML,ANTIREFLUX,E FDA UDI

Identifiers

Catalog Number
URO53211 FDA UDI
Primary DI / UDI-DI
10888277400269 FDA UDI
FDA Product Code
KNX FDA UDI
GMDN Term
Urethral catheterization support kit, urinary drainage 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urethral catheterization support kit, urinary drainage

Medline Industries, Inc. by Medline Industries, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urethral catheterization support kit, urinary drainage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e9acea8-ceaa-4b31-9271-13a663743324 35 fields · synced Jun 1, 2026