← Back to catalogue

Prognost F

EUDAMED

Class I (EU MDR)

Ref 7041-5-8704

by PROTEC X-ray Systems GmbH

Identity

Trade Name
PROGNOST F EUDAMED
Device Name
PROGNOST F EUDAMED
Model / Reference
7041-5-8704 EUDAMED

Identifiers

Primary DI / UDI-DI
04260502641910 EUDAMED
Basic UDI-DI
426050264X008ZR EUDAMED
EMDN Code
Z11030503 PATIENT TABLES FOR RADIOLOGICAL EQUIPMENT EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Prognost F by PROTEC X-ray Systems GmbH — 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

EUDAMED SRN
DE-MF-000048351

Sources (1)

  • EUDAMED 6c063ddc-2e43-4c06-8a0c-1141371d0cda 61 fields · synced Jun 19, 2026