Resolve Matrix™ Biologic Membrane

FDA UDI

Class U (US FDA UDI)

by Dsm Biomedical, Inc.

Identity

Trade Name: Resolve Matrix™ Biologic Membrane FDA UDI
Generic Name: Animal-derived wound matrix dressing FDA UDI
Device Name: Resolve Matrix™ 3 cm x 4 cm FDA UDI
Model / Reference: 30052-31 FDA UDI
Description: Resolve Matrix™ 3 cm x 4 cm FDA UDI

Identifiers

Catalog Number: RMAD34 FDA UDI
Primary DI / UDI-DI: 00812337020596 FDA UDI
FDA Product Code: KGN 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 3 Centimeter FDA UDI
Width — 4 Centimeter FDA UDI

Category: Animal-derived wound matrix dressing

Resolve Matrix™ Biologic Membrane by Dsm Biomedical, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Animal-derived wound matrix dressing.

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Solventum™ Promogran™ — Solventum US LLC · U
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class U	Pending data

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Manufacturer

Manufacturer: Dsm Biomedical, Inc.

Sources (1)

FDA UDI b06fbc1f-cfcb-4184-bc38-8c14d12825c6 37 fields · synced Jun 1, 2026