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Securlancets Unik

EUDAMED

Class IIa (EU MDR)

Ref 7639Model Type 520Ref 7638Model type 520

by HTL-Strefa S.A.

Identity

Trade Name
Securlancets Unik EUDAMED
Device Name
Safety lancet EUDAMED
Model / Reference
Type 520 EUDAMED
7639 EUDAMED
7638 EUDAMED

Identifiers

Primary DI / UDI-DI
08012992437094 EUDAMED
08012992437087 EUDAMED
Basic UDI-DI
B-08012992437094 EUDAMED
B-08012992437087 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED
France EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Blood lancet, single-use

Securlancets Unik by Htl Strefa S A — Class IIa — MDD — 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/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 21bdb9c5-913d-4267-b8bb-74f44b4213d2 61 fields · synced Jul 19, 2026
  • EUDAMED e6702b74-976e-4d31-9816-685bed9cf738 61 fields · synced May 18, 2026