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Mesh|Ex

FDA UDI

Class I (US FDA UDI)

by Exsurco Medical, Inc.

Identity

Trade Name
Mesh|Ex FDA UDI
Generic Name
Skin graft mesher FDA UDI
Device Name
ASM, Exsurco Mesher FDA UDI
Model / Reference
X101836 FDA UDI
Description
ASM, Exsurco Mesher FDA UDI

Identifiers

Catalog Number
X101836 FDA UDI
Primary DI / UDI-DI
00810006780130 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Skin graft mesher

Mesh|Ex by Exsurco Medical, Inc. — 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

Manufacturer
Exsurco Medical, Inc.

Sources (1)

  • FDA UDI 41fa0bb1-78fc-4c5d-a8de-91de24a80cd4 36 fields · synced Jun 8, 2026