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Safety Lancet

EUDAMED

Class IIa (EU MDR)

Ref 94-4918-26SModel PA 26G

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Device Name
Safety Lancet EUDAMED
Model / Reference
PA 26G EUDAMED
94-4918-26S EUDAMED

Identifiers

Primary DI / UDI-DI
06949517006669 EUDAMED
Basic UDI-DI
B-06949517006669 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

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 e9d8b387-5c98-4cb9-9c22-d5d92490e6a4 61 fields · synced May 25, 2026