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AutoCheck

EUDAMED

Class IIa (EU MDR)

Ref I

by Beijing Ruicheng Medical Supplies Co., Ltd.

Identity

Trade Name
AutoCheck EUDAMED
Device Name
Lancet EUDAMED
Model / Reference
I EUDAMED

Identifiers

Primary DI / UDI-DI
06950423216028 EUDAMED
Basic UDI-DI
69504232IT2 EUDAMED
Direct Marketing DI
06950423216028 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

AutoCheck by Beijing Ruicheng Medical Supplies 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

EUDAMED SRN
CN-MF-000002282
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 90e493de-42ee-4885-9821-4bdb11db524e 61 fields · synced Oct 6, 2026