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Lazzaned Group

EUDAMED

Class IIa (EU MDR)

Ref PA 23G 2.2mmModel PA PA2 NPA APA

by Shandong Lianfa Medical Plastic Products Co., Ltd.

Identity

Trade Name
LAZZANED GROUP EUDAMED
Device Name
safety lancets EUDAMED
Model / Reference
PA PA2 NPA APA EUDAMED
PA 23G 2.2mm EUDAMED

Identifiers

Primary DI / UDI-DI
06949517007987 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
Italy 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

Lazzaned Group 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

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Manufacturer

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

Sources (1)

  • EUDAMED b5261a38-73c9-4e9a-bd2b-b1de299b3c18 61 fields · synced Jun 18, 2026