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Optilet PRO nakłuwacz

EUDAMED

Class I (EU MDR)

Ref 5222Model Optilet PRO, Optilet MINI

by Diagnosis S.a.

Identity

Trade Name
Optilet PRO nakłuwacz EUDAMED
Device Name
Lancing device EUDAMED
Model / Reference
Optilet PRO, Optilet MINI EUDAMED
5222 EUDAMED

Identifiers

Primary DI / UDI-DI
05907581259306 EUDAMED
Basic UDI-DI
590758125lancetdeviceAZ EUDAMED
EMDN Code
A018099 NEEDLES - OTHER ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Category: Electromagnetic surgical navigation device tracking system

Optilet PRO nakłuwacz by Diagnosis S.a. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic surgical navigation device tracking system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Diagnosis S.a.
EUDAMED SRN
PL-MF-000014187

Sources (1)

  • EUDAMED 6a88d0ac-a3d7-4251-9b4e-c546e3ab3bed 61 fields · synced Jul 13, 2026