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4Med

FDA UDI

Class I (US FDA UDI)

by 4 Med Ltd

Identity

Trade Name
4Med FDA UDI
Generic Name
Skin graft carrier FDA UDI
Device Name
Skin Graft Carrier 35 cm FDA UDI
Model / Reference
9910102-35 FDA UDI
Description
Skin Graft Carrier 35 cm FDA UDI

Identifiers

Primary DI / UDI-DI
07290018281123 FDA UDI
FDA Product Code
GEJ FDA UDI
GMDN Term
Skin graft carrier 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 35 Centimeter FDA UDI

Category: Skin graft carrier

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

Similar devices

Also classified as Skin graft carrier.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
4 Med Ltd

Sources (1)

  • FDA UDI 6db4a456-ce01-4353-b1e6-298ed0e47109 36 fields · synced Jun 8, 2026