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Prognost F

EUDAMED

Class I (EU MDR)

Ref 7041-5-8703

by PROTEC X-ray Systems GmbH

Identity

Trade Name
PROGNOST F EUDAMED
Device Name
PROGNOST F EUDAMED
Model / Reference
7041-5-8703 EUDAMED

Identifiers

Primary DI / UDI-DI
04260502641903 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

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Manufacturer

EUDAMED SRN
DE-MF-000048351

Sources (1)

  • EUDAMED 382b1777-d577-40bc-b531-2becf2d37fdd 61 fields · synced Jun 19, 2026