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Gima

EUDAMED

Class IIa (EU MDR)

Ref PA-21G 2.2mmModel PA PA2 NPA APA

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Trade Name
GIMA EUDAMED
Device Name
safety lancets EUDAMED
Model / Reference
PA PA2 NPA APA EUDAMED
PA-21G 2.2mm EUDAMED

Identifiers

Primary DI / UDI-DI
06949517008281 EUDAMED
Basic UDI-DI
69495170PAHH 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

Gima by Shandong Lianfa Medical Plastic Products Co., Ltd. — 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-000028790
Authorised Representative
Linkfar Healthcare GmbH DE-AR-000005107

Sources (1)

  • EUDAMED fa8bc1a2-dcf5-45d7-aae6-7256254006a0 61 fields · synced Jun 18, 2026