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MiniDock Ultra

EUDAMED

Class A (EU MDR)

Ref PM001 Ultra

by Guangzhou Pluslife Biotech Co., Ltd

Identity

Trade Name
MiniDock Ultra EUDAMED
Device Name
Integrated Nucleic Acid Testing Device EUDAMED
Model / Reference
PM001 Ultra EUDAMED

Identifiers

Primary DI / UDI-DI
06975327120639 EUDAMED
Basic UDI-DI
697532712PM001UFG EUDAMED
Direct Marketing DI
06975327120639 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS 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

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid sample preparation instrument IVD

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

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

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
PureCE B.V. NL-AR-000006069

Sources (1)

  • EUDAMED 6fdf84f7-2cf1-4d9a-bed5-59829d4e309b 61 fields · synced Jun 19, 2026