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Medline

FDA UDI

Class U (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Exudate-absorbent first aid dressing, hydrophilic-gel, antimicrobial FDA UDI
Device Name
REINFORCED,GELFIBER,OPTICELL AG+, .75X18 FDA UDI
Model / Reference
MSC9818R FDA UDI
Description
REINFORCED,GELFIBER,OPTICELL AG+, .75X18 FDA UDI

Identifiers

Catalog Number
MSC9818R FDA UDI
Primary DI / UDI-DI
10888277675605 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Exudate-absorbent first aid dressing, hydrophilic-gel, antimicrobial FDA UDI

Classification

Device Class
U 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

Yes

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: Exudate-absorbent first aid dressing, hydrophilic-gel, antimicrobial

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

Similar devices

Also classified as Exudate-absorbent first aid dressing, hydrophilic-gel, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 5402d62f-f33d-4a7a-b839-7159a587fd25 36 fields · synced May 30, 2026