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Gelseal™ Cardiovascular Patch

FDA UDI

Class II (US FDA UDI)

by Vascutek Ltd

Identity

Trade Name
Gelseal™ Cardiovascular Patch FDA UDI
Generic Name
Cardiovascular patch, animal-derived FDA UDI
Device Name
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch FDA UDI
Model / Reference
951010 FDA UDI
Description
Gelseal Gelatin Impregnated Knitted Cardiovascular Patch FDA UDI

Identifiers

Catalog Number
951010 FDA UDI
Primary DI / UDI-DI
05037881010427 FDA UDI
510(k) Number
K200955 FDA UDI
K963611 FDA UDI
FDA Product Code
DXZ FDA UDI
GMDN Term
Cardiovascular patch, animal-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3470 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cardiovascular patch, animal-derived

Gelseal™ Cardiovascular Patch by Vascutek Ltd — 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

Manufacturer
Vascutek Ltd

Sources (1)

  • FDA UDI 2b15e1f3-e037-4a20-a1e0-c83621d86805 38 fields · synced Jun 1, 2026