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Hair transplant guide device

EUDAMED

Class I (EU MDR)

Ref MHT223D-10

by OHDAE Corporation

Identity

Device Name
Hair transplant guide device EUDAMED
Model / Reference
MHT223D-10 EUDAMED

Identifiers

Primary DI / UDI-DI
08800181200297 EUDAMED
Basic UDI-DI
B-08800181200297 EUDAMED
EMDN Code
K01020114 MINIMALLY INVASIVE SURGERY GUIDES, SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Category: Orthopaedic prosthesis implantation positioning instrument, single-use

Hair transplant guide device by OHDAE Corporation — Class I — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
OHDAE Corporation
EUDAMED SRN
KR-MF-000025038
Authorised Representative
AeMi World e.K DE-AR-000007704

Sources (1)

  • EUDAMED 3dc6ce4c-c2a8-497b-b42e-6d13f1e07ca4 61 fields · synced Oct 7, 2026