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Brennen Skin Graft Mesher

FDA UDI

Class I (US FDA UDI)

by Stellen Medical, LLC

Identity

Trade Name
Brennen Skin Graft Mesher FDA UDI
Generic Name
Skin graft mesher FDA UDI
Device Name
The Skin Graft Mesher is a surigical instrument designed to expand skin grafts. FDA UDI
Model / Reference
PC FDA UDI
Description
The Skin Graft Mesher is a surigical instrument designed to expand skin grafts. FDA UDI

Identifiers

Primary DI / UDI-DI
00855638007194 FDA UDI
FDA Product Code
FZW FDA UDI
GMDN Term
Skin graft mesher FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Skin graft mesher

Brennen Skin Graft Mesher by Stellen Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin graft mesher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6ee3b17c-260f-446c-85b5-85667efdb5d0 34 fields · synced Jun 8, 2026