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VENADO Carbonate Apatite Strip

FDA UDI

Class II (US FDA UDI)

by Collagen Matrix, Inc.

Identity

Trade Name
VENADO Carbonate Apatite Strip FDA UDI
Generic Name
Composite bone graft FDA UDI
Device Name
Carbonate Apatite Strip 20cc (12.5 x 2 x 0.4cm, 2 Strips) FDA UDI
Model / Reference
4817-T122202 FDA UDI
Description
Carbonate Apatite Strip 20cc (12.5 x 2 x 0.4cm, 2 Strips) FDA UDI

Identifiers

Primary DI / UDI-DI
10813954021994 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Composite bone graft FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 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: Composite bone graft

VENADO Carbonate Apatite Strip by Collagen Matrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Composite bone graft.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Collagen Matrix, Inc.

Sources (1)

  • FDA UDI 96ef62e3-fa92-4445-b28d-819fbf2378f0 34 fields · synced Jun 8, 2026