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Hemacarotid Patch

FDA UDI

Class II (US FDA UDI)

by Intervascular, Inc.

Identity

Trade Name
Hemacarotid Patch FDA UDI
Generic Name
Cardiovascular patch, animal-derived FDA UDI
Device Name
Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch FDA UDI
Model / Reference
HEK06/120CPUT (1) FDA UDI
Description
Hemacarotidpatch Knitted Ultrathin Collagen Coated Vascular Patch FDA UDI

Identifiers

Catalog Number
HEK06/120CPUT (1) FDA UDI
Primary DI / UDI-DI
00384401010708 FDA UDI
510(k) Number
K983819 FDA UDI
FDA Product Code
DSY FDA UDI
GMDN Term
Cardiovascular patch, animal-derived FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3450 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 — 6 Millimeter FDA UDI
Length — 120 Millimeter FDA UDI

Category: Cardiovascular patch, animal-derived

Hemacarotid Patch by Intervascular, 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

Manufacturer
Intervascular, Inc.

Sources (1)

  • FDA UDI 33d5a905-910e-4b6e-b1d6-2fa927bfbdcf 38 fields · synced Jun 8, 2026