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Safety Lancet

EUDAMED

Class IIa (EU MDR)

Ref LF/03-02Model PA 21G

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Trade Name
Safety Lancet EUDAMED
Device Name
Safety Lancet EUDAMED
Model / Reference
PA 21G EUDAMED
LF/03-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06949517006645 EUDAMED
Basic UDI-DI
B-06949517006645 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Blood lancet, single-use

Safety Lancet by Shandong Lianfa Medical Plastic Products CO., LTD — Class IIa — MDD — 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/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000028790
Authorised Representative
Linkfar Healthcare GmbH DE-AR-000005107

Sources (1)

  • EUDAMED 167eb61c-dc83-4b55-a7eb-c7e38962979c 61 fields · synced May 27, 2026