Skip to content

syngo.via RT Image Suite 11664618

by Siemens Healthcare GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04068151011388 UDI-DIDate18 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
syngo.via RT Image Suite
Generic Name
Full-body CT system
Model / Reference
11664618
Primary DI / UDI-DI
04068151011388
510(k) Number
FDA Product Code
MUJ
GMDN Term
Full-body CT system
Device Class
Class II
Regulation Number
892.5050
GUDID distribution status
In Commercial Distribution

Other devices from Siemens Healthcare

See all devices from Siemens Healthcare →

Properties

  • Serial Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No