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Almag Active

EUDAMED

Class IIa (EU MDR)

Ref 13491

by Yelatma Instrument-Making Enterprise Joint-Stock Company

Identity

Trade Name
ALMAG ACTIVE EUDAMED
Device Name
ALMAG ACTIVE EUDAMED
Model / Reference
13491 EUDAMED

Identifiers

Primary DI / UDI-DI
D-4602122003103LU32 EUDAMED
Basic UDI-DI
B-4602122003103LU32 EUDAMED
EMDN Code
Z120606 MAGNETOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Almag Active by Yelatma Instrument-Making Enterprise Joint-Stock Company — Class IIa — 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

EUDAMED SRN
RU-MF-000008411
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 4ec50e4c-02c9-4522-aa43-aa02b1f88a7c 61 fields · synced Oct 6, 2026