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Mueller More Skin

FDA UDI

Class I (US FDA UDI)

by Mueller Sports Medicine, Inc.

Identity

Trade Name
Mueller More Skin FDA UDI
Generic Name
Wound hydrogel dressing, non-antimicrobial FDA UDI
Device Name
MORE SKIN, 12" X 12" SHEET FDA UDI
Model / Reference
131404 FDA UDI
Description
MORE SKIN, 12" X 12" SHEET FDA UDI

Identifiers

Catalog Number
131404 FDA UDI
Primary DI / UDI-DI
00074676131443 FDA UDI
FDA Product Code
NAE FDA UDI
GMDN Term
Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4022 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

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Width — 12 Inch FDA UDI
Length — 12 Inch FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Mueller More Skin by Mueller Sports Medicine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3d2ff0e4-0100-474e-9b49-afae02c0e8b5 36 fields · synced Jun 9, 2026