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DuraGen®

FDA UDI

Class II (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
DuraGen® FDA UDI
Generic Name
Dura mater graft, bovine FDA UDI
Device Name
DuraGen® Dural Graft Matrix 4 in x 5 in (10cm x12.5cm) FDA UDI
Model / Reference
ID4501 FDA UDI
Description
DuraGen® Dural Graft Matrix 4 in x 5 in (10cm x12.5cm) FDA UDI

Identifiers

Catalog Number
ID4501 FDA UDI
Primary DI / UDI-DI
10381780023616 FDA UDI
510(k) Number
K982180 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

DuraGen® by Integra Lifesciences Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dura mater graft, bovine.

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 69b8f693-ecb4-4d08-a7fd-65a6b5059007 38 fields · synced Jun 8, 2026