Rtm 80 H

by I.A.E. Industria Applicazioni Elettroniche S.P.A. 2 variants

Ref RTM 80 H 0.3/0.5

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number805930749385G4 Basic UDI-DI 08059307491549UDI-DI	Date12 May 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: X-ray tubes
Model / Reference: RTM 80 H 0.3/0.5

Primary DI / UDI-DI: 08059307491549
Basic UDI-DI: 805930749385G4
Direct Marketing DI: 08059307491549
EMDN Code: Z11039099 Various radiodiagnostic and interventional instruments – other

Device Class: Class IIb
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000021626

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No