CANON INC.

GUDID 04549292075182

CANON INC.

Stationary general-purpose fluoroscopic x-ray system, digital
Primary Device ID04549292075182
NIH Device Record Key73e621ab-03ea-4cef-9b12-ee530fd9b596
Commercial Distribution StatusIn Commercial Distribution
Brand NameCANON INC.
Version Model NumberCSX-20
Company DUNS695138065
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104549292075182 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OWBInterventional Fluoroscopic X-Ray System

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 Date2016-09-24

On-Brand Devices [CANON INC.]

04960999999708CXDI-801C Wireless
04960999999043CXDI-401C Wireless
04960999989600CXDI-701C Wireless
04960999988184CXDI-55C
04960999974965CXDI-70C Wireless
04960999814735CXDI-501C
04960999814728CXDI-501G
04960999812601CXDI-401G COMPACT
04960999810911CXDI-50RF
04549292099478CXDI-410C Wireless
04549292099454CXDI-810C Wireless
04549292099447CXDI-710C Wireless
04549292075182CSX-20
04549292075175CSX-30
04549292074369TX-20
04549292074352RK-F2
04549292074345CX-1
04549292074338CR-2 Plus AF
04549292074321CR-2 AF
04549292049695CXDI-401C COMPACT
04549292084696Ophthalmic Software Platform RX
04549292168679CXDI-402C Wireless
04549292167436CXDI-702C Wireless
04549292182729imageSPECTRUM
04549292200935CXDI-Pro
04549292200942CXDI-Elite
04549292228489CR-10

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