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Verifine

EUDAMED

Class IIa (EU MDR)

Ref HB-100

by Promisemed Hangzhou Meditech Co., Ltd.

Identity

Trade Name
Verifine EUDAMED
Device Name
Heel Blood Lancet EUDAMED
Model / Reference
HB-100 EUDAMED

Identifiers

Primary DI / UDI-DI
06971227401915 EUDAMED
Basic UDI-DI
697122740HBX7 EUDAMED
Unit of Use DI
86971227401911 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Greece 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

Verifine by Promisemed Hangzhou Meditech Co., Ltd. — Class IIa — 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-000008465
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED c71e4042-8b8d-49a1-83fe-d25f41c89843 61 fields · synced May 23, 2026