CT SCANNER

GUDID 04987670104701

CANON INC.

Full-body CT system
Primary Device ID04987670104701
NIH Device Record Key7c76774d-fb6c-4278-9b5a-3c5a5e488917
Commercial Distribution StatusIn Commercial Distribution
Brand NameCT SCANNER
Version Model NumberTSX-501R
Company DUNS690549662
Company NameCANON INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx
Phone+1-8004211968
Emailxxx@xxx.xxx

Device Identifiers

Device Issuing AgencyDevice ID
GS104987670104701 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JAKSystem, X-Ray, Tomography, Computed

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-09
Device Publish Date2026-03-01

On-Brand Devices [CT SCANNER]

04987670106538TSX-301B
04987670104701TSX-501R

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.