← Back to catalogue

Solofix Safety

EUDAMED

Class IIa (EU MDR)

Ref 7132Model Type 553-556

by HTL-Strefa S.A.

Identity

Trade Name
Solofix Safety EUDAMED
Solofix® Safety EUDAMED
Device Name
Safety lancet EUDAMED
Model / Reference
Type 553-556 EUDAMED
7132 EUDAMED

Identifiers

Primary DI / UDI-DI
05903999603281 EUDAMED
Basic UDI-DI
5907996095535563D EUDAMED
B-05903999603281 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Denmark 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

Solofix Safety by Htl Strefa S A — Class IIa — MDD, 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/MDD

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 099d98de-f182-4051-8fca-68901f3b67df 61 fields · synced Jun 19, 2026
  • EUDAMED bea93667-3e26-4696-b8cc-c448943eca81 61 fields · synced Jun 11, 2026