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Pluslife Thermolyse

EUDAMED

Class A (EU MDR)

Ref WD002

by Guangzhou Pluslife Biotech Co., Ltd

Identity

Device Name
Pluslife Thermolyse EUDAMED
Model / Reference
WD002 EUDAMED

Identifiers

Primary DI / UDI-DI
06975327120615 EUDAMED
Basic UDI-DI
697532712WD002G7 EUDAMED
Direct Marketing DI
06975327120615 EUDAMED
EMDN Code
W02079080 VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Pluslife Thermolyse by Guangzhou Pluslife Biotech Co., Ltd — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000025784
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 76650408-1218-44f3-b333-4e497e241379 61 fields · synced Jun 19, 2026