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Integra® Dermal Regeneration Template

FDA UDI

Class III (US FDA UDI)

by Integra Lifesciences Corp.

Identity

Trade Name
Integra® Dermal Regeneration Template FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
Integra® Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) FDA UDI
Model / Reference
34051 FDA UDI
Description
Integra® Dermal Regeneration Template 4in. x 5in. (10cm x 12.5cm) FDA UDI

Identifiers

Catalog Number
34051 FDA UDI
Primary DI / UDI-DI
10381780000563 FDA UDI
PMA Number
P900033 FDA UDI
FDA Product Code
MGR FDA UDI
MDD FDA UDI
GMDN Term
Animal-derived wound matrix dressing FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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: Animal-derived wound matrix dressing

Integra® Dermal Regeneration Template by Integra Lifesciences Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Animal-derived wound matrix dressing.

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 fd011b83-1956-4f6f-b1ed-9f39ed5935f6 38 fields · synced Jun 8, 2026