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Lancing device

EUDAMED

Class I (EU MDR)

Ref NoModel HH-X-T,HH-XIII-T,HH-XV-T,HH-XVI-T,HH-XVII-T,HH-XVIII-T,HH-XIX,HH-XXI-T,HH-XXII-T,HH-XXIII-T,HH-XXIV-T,HH-XXV-T, HH-XXVI-T, HH-XXVII-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XXXI-T,HH-XXXII-T

by Tianjin Huahong Technology Co., Ltd.

Identity

Device Name
Lancing device EUDAMED
Model / Reference
HH-X-T,HH-XIII-T,HH-XV-T,HH-XVI-T,HH-XVII-T,HH-XVIII-T,HH-XIX,HH-XXI-T,HH-XXII-T,HH-XXIII-T,HH-XXIV-T,HH-XXV-T, HH-XXVI-T, HH-XXVII-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XXXI-T,HH-XXXII-T EUDAMED
No EUDAMED

Identifiers

Primary DI / UDI-DI
06957138611520 EUDAMED
Basic UDI-DI
69571386LD03U5 EUDAMED
EMDN Code
W0501010299 CAPILLARY BLOOD COLLECTION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

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

Lancing device by Tianjin Huahong Technology Co., Ltd. — Class I — 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-000015849
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 489f787c-b843-4062-bc4c-63327239a9e1 61 fields · synced May 23, 2026