← Back to catalogue

Monoclix

EUDAMED

Class IIa (EU MDR)

Ref "SOFT 28G C2 85022S"

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
MONOCLIX EUDAMED
Device Name
Disposable Blood Lancets EUDAMED
Model / Reference
"SOFT 28G C2 85022S" EUDAMED

Identifiers

Primary DI / UDI-DI
16945630135269 EUDAMED
Basic UDI-DI
6945630101B9 EUDAMED
Unit of Use DI
06945630135262 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

Yes

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

Monoclix by Sterilance Medical (Suzhou) Inc. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000002860
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED dbf4eabe-c850-4727-bd9b-03e513e7d676 61 fields · synced Jun 19, 2026