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MenaLancet Pro

EUDAMED

Class IIa (EU MDR)

Ref 7254Model Type 520Ref 7154

by HTL-Strefa S.A.

Identity

Trade Name
MenaLancet Pro EUDAMED
Device Name
Safety lancet EUDAMED
Model / Reference
Type 520 EUDAMED
7254 EUDAMED
7154 EUDAMED

Identifiers

Primary DI / UDI-DI
08426521421223 EUDAMED
08426521421230 EUDAMED
Basic UDI-DI
B-08426521421223 EUDAMED
B-08426521421230 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

MenaLancet Pro 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 1a90105f-27d6-48fa-bad6-8a3da857968f 61 fields · synced Jul 29, 2026
  • EUDAMED 4c67ebeb-77c4-41bd-8dde-467b9691ac2d 61 fields · synced May 18, 2026