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Acti-Lance

EUDAMED

Class IIa (EU MDR)

Ref 9227Model Type 610

by HTL-Strefa S.A.

Identity

Trade Name
Acti-Lance EUDAMED
Device Name
Safety Lancet EUDAMED
Model / Reference
Type 610 EUDAMED
9227 EUDAMED

Identifiers

Primary DI / UDI-DI
05903999608248 EUDAMED
Basic UDI-DI
590799609610MF EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Acti-Lance by Htl Strefa S A — 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

Manufacturer
HTL-Strefa S.A.
EUDAMED SRN
PL-MF-000002198

Sources (1)

  • EUDAMED d2516861-4678-4bff-9e41-47d07176e0ab 61 fields · synced May 23, 2026