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GimaLancet

EUDAMED

Class IIa (EU MDR)

Ref Press plus 23G 1.8mmRef Press plus 21G 2.2mm

by Sterilance Medical (Suzhou) Inc.

Identity

Trade Name
GimaLancet EUDAMED
Device Name
Disposable Safety Lancets EUDAMED
Model / Reference
Press plus 23G 1.8mm EUDAMED
Press plus 21G 2.2mm EUDAMED

Identifiers

Primary DI / UDI-DI
16945630137003 EUDAMED
16945630136983 EUDAMED
Basic UDI-DI
6945630105BH EUDAMED
Unit of Use DI
06945630137006 EUDAMED
06945630136986 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

GimaLancet 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 (2)

  • EUDAMED c7f8ea23-f81c-4778-a731-ee45a4eb63f4 61 fields · synced Jul 9, 2026
  • EUDAMED a6f9357b-fb18-4b09-a68a-8bf6bdeb643f 61 fields · synced May 19, 2026