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Lancet

EUDAMED

Class IIa (EU MDR)

Ref XLIII30Model XLIIIModel XLIII-30

by Hebei Xinle Sci&Tech Co., Ltd

Identity

Trade Name
Lancet EUDAMED
xinle EUDAMED
Device Name
Lancet EUDAMED
Model / Reference
XLIII EUDAMED
XLIII30 EUDAMED
XLIII-30 EUDAMED

Identifiers

Primary DI / UDI-DI
06950383615169 EUDAMED
Basic UDI-DI
69503836XL0202IMQ4 EUDAMED
B-06950383615169 EUDAMED
Unit of Use DI
86950383615165 EUDAMED
EMDN Code
V010402 LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Lancet by Hebei Xinle Sci&Tech Co., Ltd. — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000016692
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (2)

  • EUDAMED c9be094b-7307-4d4a-82df-44bd7da814a3 61 fields · synced Jul 26, 2026
  • EUDAMED fb1b427e-9fb6-47c0-918a-2f045b44bf90 61 fields · synced May 19, 2026