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Promogran®

FDA UDI

Class U (US FDA UDI)

by Systagenix Wound Management, Limited

Identity

Trade Name
PROMOGRAN® FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
Matrix Wound Dressing FDA UDI
Model / Reference
PG019 FDA UDI
Description
Matrix Wound Dressing FDA UDI

Identifiers

Catalog Number
PG019 FDA UDI
Primary DI / UDI-DI
15051978003090 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Animal-derived wound matrix dressing FDA UDI

Classification

Device Class
U 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

Dimensions & Sizes

Size
Area/Surface Area — 123 Square centimeter FDA UDI

Category: Animal-derived wound matrix dressing

Promogran® by Systagenix Wound Management, Limited — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Animal-derived wound matrix dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f5d7cff8-8ef7-49d3-8d03-5b893b2e4cdd 36 fields · synced Jun 6, 2026