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Verifine

EUDAMED

Class IIa (EU MDR)

Ref SL-28-15Model Type A, Type B, Type C, Type T, Type M

by Promisemed Hangzhou Meditech Co., Ltd.

Identity

Trade Name
Verifine EUDAMED
Device Name
Safety Blood Lancets EUDAMED
Model / Reference
Type A, Type B, Type C, Type T, Type M EUDAMED
SL-28-15 EUDAMED

Identifiers

Primary DI / UDI-DI
06971227401052 EUDAMED
Basic UDI-DI
697122740SLYU EUDAMED
Unit of Use DI
86971227401058 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Sweden 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

Verifine by Promisemed Hangzhou Meditech 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-000008465
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 65901013-3e2c-4c6d-b350-041fc17fba21 61 fields · synced May 23, 2026