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Mepiform®

FDA UDI

Class I (US FDA UDI)

by Mölnlycke Health Care AB

Identity

Trade Name
Mepiform® FDA UDI
Generic Name
Scar management dressing, single-use, sterile FDA UDI
Device Name
Mepiform 10x18 cm FDA UDI
Model / Reference
293499 FDA UDI
Description
Mepiform 10x18 cm FDA UDI

Identifiers

Primary DI / UDI-DI
07323190308323 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar management dressing, single-use, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4025 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scar management dressing, single-use, sterile

Mepiform® by Mölnlycke Health Care AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scar management dressing, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mölnlycke Health Care AB

Sources (1)

  • FDA UDI 4eefd07f-1024-4c57-ba13-edb5c2ecf95c 35 fields · synced May 30, 2026