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Micrograft gauze + cork plate, 1:3

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 2.3/1

by Humeca B.V.

Identity

Trade Name
Micrograft gauze + cork plate, 1:3 FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
Micrograft gauze + cork plate, 1:3 EUDAMED
Model / Reference
2.3/1 EUDAMEDFDA UDI

Identifiers

Catalog Number
2.3/1 FDA UDI
Primary DI / UDI-DI
08717903490013 EUDAMEDFDA UDI
Basic UDI-DI
B-08717903490013 EUDAMED
FDA Product Code
GFD FDA UDI
EMDN Code
M0299 GAUZES - OTHER EUDAMED
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4820 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Micrograft gauze + cork plate, 1:3 by Humeca B.V. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Humeca B.V.
EUDAMED SRN
NL-MF-000010933

Sources (2)

  • EUDAMED 1ba5310e-3bce-40ca-b654-43af45c48945 61 fields · synced Jun 18, 2026
  • FDA UDI eb21ee57-8f2a-4e83-b335-29af4ffa526c 33 fields · synced May 30, 2026