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Prolance

EUDAMED

Class IIa (EU MDR)

Ref 8478Model type 430

by HTL-Strefa S.A.

Identity

Trade Name
Prolance EUDAMED
Device Name
safety lancet EUDAMED
Model / Reference
type 430 EUDAMED
8478 EUDAMED

Identifiers

Primary DI / UDI-DI
05907996098835 EUDAMED
Basic UDI-DI
B-05907996098835 EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Lithuania 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

Prolance 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 (1)

  • EUDAMED a1210a44-d559-4fc5-8492-5252e7a661d6 61 fields · synced May 23, 2026