← Back to catalogue

linkfar

EUDAMED

Class IIa (EU MDR)

Ref PA 30G 1.5mmModel PA PA2 NPA APARef PA-30G 1.5mm

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Trade Name
linkfar EUDAMED
Device Name
safety lancets EUDAMED
Model / Reference
PA PA2 NPA APA EUDAMED
PA 30G 1.5mm EUDAMED
PA-30G 1.5mm EUDAMED

Identifiers

Primary DI / UDI-DI
06949517008243 EUDAMED
06949517008137 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
Germany 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

linkfar 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 6a805e63-cd52-4140-a7a2-ecc91dcf8267 61 fields · synced Oct 6, 2026
  • EUDAMED bd733237-1c31-4197-92ff-d3acf351710c 61 fields · synced May 17, 2026