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D42 dermatome set

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 4.D42STS

by Humeca B.V.

Identity

Trade Name
D42 dermatome set FDA UDI
Generic Name
Dermatome handpiece, electrically-powered FDA UDI
Device Name
D42 dermatome set EUDAMED
Model / Reference
4.D42STS EUDAMEDFDA UDI

Identifiers

Catalog Number
4.D42STS FDA UDI
Primary DI / UDI-DI
08717903490358 EUDAMEDFDA UDI
Basic UDI-DI
B-08717903490358 EUDAMED
FDA Product Code
GFD FDA UDI
EMDN Code
L0103 DERMOTOMES AND BLADES, REUSABLE EUDAMED
GMDN Term
Dermatome handpiece, electrically-powered FDA UDI

Classification

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

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

D42 dermatome set by Humeca B.V. — Class IIa — 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 bddd23bf-97c6-4e5f-89fe-b90020841c7c 61 fields · synced Jul 10, 2026
  • FDA UDI 3fb62665-9b44-4245-9c1d-7be49d3992cc 34 fields · synced May 30, 2026