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Safety lancet

EUDAMED

Class IIa (EU MDR)

Ref NoModel XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVIII, XXX, XXXIV, XXXVI

by Tianjin Huahong Technology Co., Ltd.

Identity

Device Name
Safety lancet EUDAMED
Model / Reference
XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVIII, XXX, XXXIV, XXXVI EUDAMED
No EUDAMED

Identifiers

Primary DI / UDI-DI
06957138609176 EUDAMED
Basic UDI-DI
69571386SL02WU EUDAMED
Unit of Use DI
56957138609171 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

Safety lancet by Tianjin Huahong Technology 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-000015849
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 6c3a91d9-dd40-443e-8134-9c71a34cf4af 61 fields · synced May 23, 2026