← Back to catalogue

Primo Pro

EUDAMED

Class I (EU MDR)

Ref 034-998Model Primo Pro

by Possum Ltd.

Identity

Trade Name
Primo Pro EUDAMED
Device Name
Primo Pro EUDAMED
Model / Reference
Primo Pro EUDAMED
034-998 EUDAMED

Identifiers

Primary DI / UDI-DI
05061067720015 EUDAMED
Basic UDI-DI
5061067PrimoProP4 EUDAMED
EMDN Code
Y241203 PROGRAMMABLE REMOTE CONTROLS, HOME AUTOMATION SYSTEMS, CONTROL SATELLITES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Primo Pro by Possum Ltd. — 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
Possum Ltd.
EUDAMED SRN
UK-MF-000051816
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 98b826a8-c94d-4738-a287-a0c56bd71db6 61 fields · synced Jun 18, 2026