← Back to catalogue

Stymulator Campbella

EUDAMED

Class I (EU MDR)

Ref SW-1

by MDT sp. z o.o.

Identity

Trade Name
Stymulator Campbella EUDAMED
Device Name
Campbell Stimulator / Stymulator Campbella EUDAMED
Model / Reference
SW-1 EUDAMED

Identifiers

Primary DI / UDI-DI
05907642694909 EUDAMED
Basic UDI-DI
5907642694SW1HC EUDAMED
Direct Marketing DI
05907642694909 EUDAMED
EMDN Code
Q0209 STRABISMUS DEVICES 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

Stymulator Campbella 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
MDT sp. z o.o.
EUDAMED SRN
PL-MF-000009248

Sources (1)

  • EUDAMED a4134a27-6067-4650-bc37-845e0072ecbb 61 fields · synced Jul 19, 2026