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Blood Lancets

EUDAMED

Class IIa (EU MDR)

Ref Ⅱ-30GModel Ⅰ Ⅱ Ⅲ

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Device Name
Blood Lancets EUDAMED
Model / Reference
Ⅰ Ⅱ Ⅲ EUDAMED
Ⅱ-30G EUDAMED

Identifiers

Primary DI / UDI-DI
06949517007369 EUDAMED
06949517007901 EUDAMED
Basic UDI-DI
694951700V8 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT 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

Blood Lancets by Shandong Lianfa Medical Plastic Products Co., Ltd. — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

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 (2)

  • EUDAMED f236cca7-1ad1-451b-9bdd-b32fbfcb7a29 61 fields · synced Oct 6, 2026
  • EUDAMED ee252f87-85d3-4290-8d8c-a1f32b346806 61 fields · synced May 18, 2026