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Okulistyczna kaseta szkieł próbnych

EUDAMED

Class I (EU MDR)

Ref PL-232Ref BR-260

by MDT sp. z o.o.

Identity

Trade Name
Okulistyczna kaseta szkieł próbnych EUDAMED
Device Name
Ophthalmic Trial Lens Set / Okulistyczna kaseta szkieł próbnych EUDAMED
Model / Reference
PL-232 EUDAMED
BR-260 EUDAMED

Identifiers

Primary DI / UDI-DI
05907642694077 EUDAMED
05907642694060 EUDAMED
Basic UDI-DI
5907642694SETHS EUDAMED
Direct Marketing DI
05907642694077 EUDAMED
05907642694060 EUDAMED
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER 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

Okulistyczna kaseta szkieł próbnych by MDT sp. z o.o. — 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
MDT sp. z o.o.
EUDAMED SRN
PL-MF-000009248

Sources (2)

  • EUDAMED 1319936e-95fa-46d7-8f4b-dc6501629258 61 fields · synced Jul 9, 2026
  • EUDAMED f3774dd6-cf85-4129-9ba2-a0d021d071ed 61 fields · synced May 17, 2026