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Hair transplant guide device

EUDAMED

Class I (EU MDR)

Ref MHT223D-09

by OHDAE Corporation

Identity

Device Name
Hair transplant guide device EUDAMED
Model / Reference
MHT223D-09 EUDAMED

Identifiers

Primary DI / UDI-DI
08800181200280 EUDAMED
Basic UDI-DI
B-08800181200280 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

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

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 b4685c85-7a99-4fc0-9f21-3efbf643ab66 61 fields · synced Jun 19, 2026