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STERiLANCE

EUDAMED

Class IIa (EU MDR)

Ref 05D-192118 Impress Pro 21G 1.8mm

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
STERiLANCE EUDAMED
Device Name
Disposable Safety Lancets EUDAMED
Model / Reference
05D-192118 Impress Pro 21G 1.8mm EUDAMED

Identifiers

Primary DI / UDI-DI
16945630133890 EUDAMED
Basic UDI-DI
6945630105DVB EUDAMED
Unit of Use DI
06945630133893 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

STERiLANCE 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

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Manufacturer

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

Sources (1)

  • EUDAMED 18d6172d-8e9c-4571-b6ca-8b96050eaba1 61 fields · synced May 23, 2026