← Back to catalogue

Altms

EUDAMED

Class IIb (EU MDR)

Ref 0195

by REMED Co., Ltd.

Identity

Trade Name
ALTMS EUDAMED
Device Name
Transcranial Magnetic Stimulator EUDAMED
Model / Reference
0195 EUDAMED

Identifiers

Primary DI / UDI-DI
08809308380195 EUDAMED
Basic UDI-DI
8809308380195AF EUDAMED
Direct Marketing DI
08809308380195 EUDAMED
EMDN Code
Z12101105 MAGNETIC STIMULATORS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Romania EUDAMED

Clinical & Handling

Sterile

No

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

Altms by REMED Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Unknown

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
REMED Co., Ltd.
EUDAMED SRN
KR-MF-000008128
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 58f11891-9c83-4ef6-bdef-72481bd09a4e 61 fields · synced May 30, 2026