INTERVENTIONAL ANGIOGRAPHY SYSTEM

GUDID 04987670100208

INTERVENTIONAL ANGIOGRAPHY SYSTEM

CANON MEDICAL SYSTEMS CORPORATION

Stationary angiographic x-ray system, digital
Primary Device ID04987670100208
NIH Device Record Keyb3cb6d8d-990f-4269-a716-a2249a8a21d1
Commercial Distribution StatusIn Commercial Distribution
Brand NameINTERVENTIONAL ANGIOGRAPHY SYSTEM
Version Model NumberINFX-8000F
Company DUNS690575113
Company NameCANON MEDICAL SYSTEMS CORPORATION
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104987670100208 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQBSolid state x-ray imager (flat panel/digital imager)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-01

On-Brand Devices [INTERVENTIONAL ANGIOGRAPHY SYSTEM]

04987670100222INTERVENTIONAL ANGIOGRAPHY SYSTEM
04987670100215INTERVENTIONAL ANGIOGRAPHY SYSTEM
04987670100208INTERVENTIONAL ANGIOGRAPHY SYSTEM
04987670100192INTERVENTIONAL ANGIOGRAPHY SYSTEM

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.