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CardioCel VSD

FDA UDI

Class II (US FDA UDI)

by Admedus Regen Pty Ltd

Identity

Trade Name
CardioCel VSD FDA UDI
Generic Name
Cardiovascular patch, animal-derived FDA UDI
Device Name
The CardioCel device is a cardiovascular patch prepared from glutaraldehyde-crosslinked bovine pericardium using ADAPT TEP technology. It is a sterile, off-white, moist, pre-cut, flat sheet of acellular collagen. FDA UDI
Model / Reference
UC0202 FDA UDI
Description
The CardioCel device is a cardiovascular patch prepared from glutaraldehyde-crosslinked bovine pericardium using ADAPT TEP technology. It is a sterile, off-white, moist, pre-cut, flat sheet of acellular collagen. FDA UDI

Identifiers

Catalog Number
C0202 FDA UDI
Primary DI / UDI-DI
09348992000105 FDA UDI
510(k) Number
K130872 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 2 Centimeter FDA UDI
Length — 2 Centimeter FDA UDI

Category: Cardiovascular patch, animal-derived

CardioCel VSD by Admedus Regen Pty 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

Sources (1)

  • FDA UDI c780b474-e17a-4a04-a87e-d69b50f2e291 38 fields · synced May 30, 2026