← Back to catalogue

VITREX lab

EUDAMED

Class IIa (EU MDR)

Ref 398513 IMPRESS PRO 28G 1.8mm

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
VITREX lab EUDAMED
Device Name
Disposable Safety Lancets EUDAMED
Model / Reference
398513 IMPRESS PRO 28G 1.8mm EUDAMED

Identifiers

Primary DI / UDI-DI
16945630134002 EUDAMED
Basic UDI-DI
6945630105BH EUDAMED
Unit of Use DI
06945630134005 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

Category: Blood lancet, single-use

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

Similar devices

Also classified as Blood lancet, single-use.

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 bda79f16-b34c-4cb0-8426-85315dc0d638 61 fields · synced Jun 18, 2026