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Plusma 30

EUDAMED

Class IIa (EU MDR)

Ref PLUSMA 30

by LowTem Co., Ltd.

Identity

Trade Name
PLUSMA 30 EUDAMED
Device Name
Low temperature hydrogen peroxide sterilizers for invasive and non invasive medical device EUDAMED
Model / Reference
PLUSMA 30 EUDAMED

Identifiers

Primary DI / UDI-DI
08809416740652 EUDAMED
Basic UDI-DI
880941674C120DW EUDAMED
EMDN Code
S900199 DEVICES FOR GAS PLASMA STERILISATION (EXCLUDING CAT. D - Z) - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Plusma 30 by LowTem 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

Manufacturer
LowTem Co., Ltd.
EUDAMED SRN
KR-MF-000016177
Authorised Representative
Meridius Medical Europe Limited IE-AR-000004258

Sources (1)

  • EUDAMED 1ccc59a3-8456-4dcb-985e-5bedafa98baf 61 fields · synced Oct 6, 2026