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Blood Lancets

EUDAMED

Class IIa (EU MDR)

Ref Ⅱ30GModel Ⅰ Ⅱ Ⅲ

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Device Name
Blood Lancets EUDAMED
Model / Reference
Ⅰ Ⅱ Ⅲ EUDAMED
Ⅱ30G EUDAMED

Identifiers

Primary DI / UDI-DI
06949517007284 EUDAMED
06949517006744 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
Netherlands EUDAMED
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 1b14ec61-ca7f-4957-98be-d0a2c6f42f73 61 fields · synced Oct 6, 2026
  • EUDAMED a9606c40-72cb-4964-9378-552abac2ae6c 61 fields · synced May 19, 2026