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STERiLANCE

EUDAMED

Class IIa (EU MDR)

Ref Soft 21G

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
STERiLANCE EUDAMED
Device Name
Disposable Blood Lancets EUDAMED
Model / Reference
Soft 21G EUDAMED

Identifiers

Primary DI / UDI-DI
16945630142908 EUDAMED
Basic UDI-DI
6945630101B9 EUDAMED
Unit of Use DI
06945630142901 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa 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 398b9d36-8106-4a78-b8d8-e285ffbe99c4 61 fields · synced May 23, 2026