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Rtm 101 H 0.3/0.8

by I.A.E. Industria Applicazioni Elettroniche SpA

Rtm 101 H 0.3/0.8 is a Class I device made by I.A.E. Industria Applicazioni Elettroniche SpA, listed in FDA GUDID since 25 Aug 2020 (UDI-DI 08059307490795), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08059307490795 UDI-DI Date25 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Rtm 101 H
Generic name
X-ray system tube rotating anode assembly
Model / reference
0.3/0.8
Primary DI / UDI-DI
08059307490795
FDA product code
ITY
GMDN term
X-ray system tube rotating anode assembly
Device class
Class I
Regulation number
892.1760
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITY (Assembly, Tube Housing, X-Ray, Diagnostic).

Other devices from I.A.E. Industria Applicazioni Elettroniche SpA

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)