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Xenmatrix

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
XENMATRIX FDA UDI
Generic Name
Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial FDA UDI
Device Name
XenMatrix AB Surgical Graft, 20 cm x 40 cm FDA UDI
Model / Reference
1152040 FDA UDI
Description
XenMatrix AB Surgical Graft, 20 cm x 40 cm FDA UDI

Identifiers

Catalog Number
1152040 FDA UDI
Primary DI / UDI-DI
00801741129001 FDA UDI
FDA Product Code
OXH FDA UDI
FTM FDA UDI
PIJ FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

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
Length — 20 Centimeter FDA UDI
Width — 40 Centimeter FDA UDI

Category: Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial

Xenmatrix by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extra-gynaecological surgical mesh, collagen, bioabsorbable, antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 1ada8c21-1806-4d5d-901c-25c565277f7d 37 fields · synced May 30, 2026