← Back to catalogue

Medline

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Burn gel FDA UDI
Device Name
PLUROGEL WITH PHMB, 50G,1.75OZ TUBE FDA UDI
Model / Reference
CSG50TUBE FDA UDI
Description
PLUROGEL WITH PHMB, 50G,1.75OZ TUBE FDA UDI

Identifiers

Catalog Number
CSG50TUBE FDA UDI
Primary DI / UDI-DI
10888277723863 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Burn gel FDA UDI

Classification

Device Class
U 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Burn gel

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

Similar devices

Also classified as Burn gel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2f211e97-adc6-4ad6-b2ad-abe8b7672a9d 36 fields · synced May 31, 2026