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Cup Reader

EUDAMED

Class A (EU MDR)

Ref ACR-100

by Hangzhou Alltest Biotech.Co., Ltd.

Identity

Device Name
Cup Reader EUDAMED
Model / Reference
ACR-100 EUDAMED

Identifiers

Primary DI / UDI-DI
06936983104227 EUDAMED
Basic UDI-DI
6970277510002RYK EUDAMED
EMDN Code
W02010701 URINALYSIS (UR) - LABORATORY ANALYSERS- INSTRUMENTS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Cup Reader by Hangzhou Alltest 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-000010710
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 60b6ed38-855a-4b2c-b100-b1287131ef88 61 fields · synced Jun 18, 2026