← Back to catalogue

MemGuide

FDA UDI

Class II (US FDA UDI)

by Dsm Biomedical, Inc.

Identity

Trade Name
MemGuide FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
Porcine Dental Membrane FDA UDI
Model / Reference
30076-03 FDA UDI
Description
Porcine Dental Membrane FDA UDI

Identifiers

Catalog Number
7353040 FDA UDI
Primary DI / UDI-DI
00812337020282 FDA UDI
FDA Product Code
NPL FDA UDI
GMDN Term
Collagen dental regeneration membrane FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

Dimensions & Sizes

Size
Length — 40 Millimeter FDA UDI
Width — 30 Millimeter FDA UDI

Category: Collagen dental regeneration membrane

MemGuide by Dsm Biomedical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen dental regeneration membrane.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5b59078f-537f-4e82-addb-ae9f11df4946 35 fields · synced Jun 1, 2026