← Back to catalogue

Mepilex® Ag

FDA UDI

Class U (US FDA UDI)

by Mölnlycke Health Care AB

Identity

Trade Name
Mepilex® Ag FDA UDI
Generic Name
Wound-nonadherent dressing, absorbent, antimicrobial FDA UDI
Device Name
Mepilex Ag 10x10 cm, US FDA UDI
Model / Reference
287100 FDA UDI
Description
Mepilex Ag 10x10 cm, US FDA UDI

Identifiers

Primary DI / UDI-DI
07332430705181 FDA UDI
510(k) Number
K071354 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, 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

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

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: Wound-nonadherent dressing, absorbent, antimicrobial

Mepilex® Ag by Mölnlycke Health Care AB — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound-nonadherent dressing, absorbent, antimicrobial.

Cleared under the same submission

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 0061bf85-9e8f-4b7f-8876-e06e0a9af6db 36 fields · synced May 30, 2026