Consulting Wallah › Device Explorer › Catheters & tubes › X-ray system tube rotating anode assembly
Device Explorer · FDA GUDID · GMDN 36593

X-ray system tube rotating anode assembly

A component of an x-ray tube, the rotating anode subassembly provides the means to rotate a disc made of tungsten (W) or an alloy of tungsten at speeds above 3000 revolutions per minute while the x-ray tube is operational. The disc is contained within the vacu

US‑registered devices135in commercial distribution
Companies1labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription100%Rx‑only share
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Share of device records

I.A.E. Industria Applicazioni Elettroniche Spa135100%

Top labelers

CompanyDevicesShare
I.A.E. Industria Applicazioni Elettroniche Spa135100%

Company = labeler of record on GUDID. 1 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

RTM 780 HSRTC 1000 HSRTM 77 HRTM 77 HSXM65 TXM1016 TXM15 TXM12 TXM1016XM15XM12RTC 700 HSRTC 602 HSRTC 600 HSRTM 102 HSRTM 102 H

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
ITYAssembly, Tube Housing, X-Ray, Diagnostic135

GMDN & GCC registration

  • GMDN code 36593 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 100% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many x-ray system tube rotating anode assembly products are registered in the US?

135 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "X-ray system tube rotating anode assembly", from 1 companies. The largest labeler is I.A.E. Industria Applicazioni Elettroniche Spa with 100% of records.

Which FDA product codes apply?

ITY (Assembly, Tube Housing, X-Ray, Diagnostic)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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