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VITREX lab

EUDAMED

Class IIa (EU MDR)

Ref 397513 IMPRESS PRO 21G 1.8mm

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
VITREX lab EUDAMED
Device Name
Disposable Safety Lancets EUDAMED
Model / Reference
397513 IMPRESS PRO 21G 1.8mm EUDAMED

Identifiers

Primary DI / UDI-DI
16945630133999 EUDAMED
Basic UDI-DI
6945630105BH EUDAMED
Unit of Use DI
06945630133992 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark 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

VITREX lab 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

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Manufacturer

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

Sources (1)

  • EUDAMED 6c558b6b-00f5-487d-b4b5-f2e3e2f8c048 61 fields · synced Jun 18, 2026