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Amts

EUDAMED

Class IIa (EU MDR)

Ref Pro-Stamp 16P

by Woorhi Mechatronics Co., Ltd.

Identity

Device Name
AMTS EUDAMED
Model / Reference
Pro-Stamp 16P EUDAMED

Identifiers

Primary DI / UDI-DI
08800118100546 EUDAMED
Basic UDI-DI
88001181AMTSMC EUDAMED
EMDN Code
A019006 MESOTHERAPY NEEDLES EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Amts by Woorhi Mechatronics Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
KR-MF-000035848
Authorised Representative
SMB EUROPE SAS FR-AR-000011981

Sources (1)

  • EUDAMED c0b722c3-26f1-4a82-a5e0-60c54226aae9 61 fields · synced Jun 18, 2026