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DurAdapt

FDA UDI

Class II (US FDA UDI)

by Collagen Matrix, Inc.

Identity

Trade Name
DurAdapt FDA UDI
Generic Name
Dura mater graft, bovine FDA UDI
Device Name
Dural Graft Implant FDA UDI
Model / Reference
DFCS13 FDA UDI
Description
Dural Graft Implant FDA UDI

Identifiers

Catalog Number
DFCS13 FDA UDI
Primary DI / UDI-DI
00813954025872 FDA UDI
FDA Product Code
GXQ FDA UDI
GMDN Term
Dura mater graft, bovine FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5910 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: Dura mater graft, bovine

DurAdapt by Collagen Matrix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dura mater graft, bovine.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01c24d9f-2655-4d83-bade-61747b2d78a2 35 fields · synced Jun 8, 2026