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Purisma

EUDAMED

Class IIb (EU MDR)

Ref 1099

by Daeyang Medical Co., Ltd.

Identity

Device Name
PURISMA EUDAMED
Model / Reference
1099 EUDAMED

Identifiers

Primary DI / UDI-DI
08800092010992 EUDAMED
Basic UDI-DI
B-08800092010992 EUDAMED
EMDN Code
Z120602 PHYSIOTHERAPY EQUIPMENT EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

Purisma by Daeyang Medical Co. Ltd. — Class IIb — 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
KR-MF-000023441
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED f4ffcf2c-e257-4ff1-ac3c-1f27718a0d1c 61 fields · synced Jul 18, 2026