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droplet

EUDAMED

Class I (EU MDR)

Ref 9396Model Type 710

by HTL-Strefa S.A.

Identity

Trade Name
droplet EUDAMED
Device Name
Lancing device EUDAMED
Model / Reference
Type 710 EUDAMED
9396 EUDAMED

Identifiers

Primary DI / UDI-DI
05903999609252 EUDAMED
Basic UDI-DI
590799609710ML EUDAMED
Direct Marketing DI
05903999609252 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Hungary EUDAMED

Clinical & Handling

Sterile

No

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

droplet by Htl Strefa S A — Class I — 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 4bc55bb3-820c-407e-a713-4200f461a658 61 fields · synced May 23, 2026