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XenoSure Biologic Patch

FDA UDI

Class II (US FDA UDI)

by LeMaitre Vascular, Inc.

Identity

Trade Name
XenoSure Biologic Patch FDA UDI
Generic Name
Cardiovascular patch, animal-derived FDA UDI
Device Name
XenoSure Biologic Patch, 10cm x 16cm, eIFU FDA UDI
Model / Reference
e10P16 FDA UDI
Description
XenoSure Biologic Patch, 10cm x 16cm, eIFU FDA UDI

Identifiers

Catalog Number
e10P16 FDA UDI
Primary DI / UDI-DI
00840663106349 FDA UDI
510(k) Number
K040835 FDA UDI
FDA Product Code
FTM FDA UDI
GMDN Term
Cardiovascular patch, animal-derived 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

No

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

Category: Cardiovascular patch, animal-derived

XenoSure Biologic Patch by LeMaitre Vascular, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiovascular patch, animal-derived.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c1784a19-1e90-4e8e-a14b-1425308f095a 37 fields · synced Jun 9, 2026