4Med

FDA UDI

Class I (US FDA UDI)

by 4 Med Ltd

Identity

Trade Name: 4Med FDA UDI
Generic Name: Skin graft mesher FDA UDI
Device Name: 4Med Skin Graft Mesher Fixed ratio 1:1 FDA UDI
Model / Reference: 9916100 FDA UDI
Description: 4Med Skin Graft Mesher Fixed ratio 1:1 FDA UDI

Identifiers

Catalog Number: 9916100 FDA UDI
Primary DI / UDI-DI: 07290018281024 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Skin graft mesher

4Med by 4 Med Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin graft mesher.

Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I
Meshgraft skin expansion system — Nouvag AG · Class I
SKIN HOLDING PLATE — SONTEC INSTRUMENTS, INC. · Class I
Mesh|Ex — EXSURCO MEDICAL, INC. · Class I
Mesh|Ex — EXSURCO MEDICAL, INC. · Class I
Brennen Skin Graft Mesher — Stellen Medical, LLC · Class I
Mesh|Ex — EXSURCO MEDICAL, INC. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: 4 Med Ltd

Sources (1)

FDA UDI a3380b94-6069-47f0-badc-d9ffe3d3f4a9 35 fields · synced Jun 7, 2026