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PSKT1 - Aurora 1

EUDAMED

Class I (EU MDR)

Ref PSKT-1

by Berner Oy

Identity

Trade Name
PSKT1 - Aurora 1 EUDAMED
Device Name
Pikosystems EUDAMED
Model / Reference
PSKT-1 EUDAMED

Identifiers

Primary DI / UDI-DI
06414505184648 EUDAMED
Basic UDI-DI
6414505PST5 EUDAMED
Direct Marketing DI
06414505184648 EUDAMED
EMDN Code
Y2199 COMMUNICATION AND INFORMATION MANAGEMENT AIDS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

PSKT1 - Aurora 1 by Berner Oy — 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
Berner Oy
EUDAMED SRN
FI-MF-000007402

Sources (1)

  • EUDAMED 1af2747a-7196-45f5-8029-1ce158eeff65 61 fields · synced Jul 25, 2026