DRX Plus 2530 C Detector 8618134

GUDID 60889978618132

DRX2530C DETECTOR /MOBILE

CARESTREAM HEALTH, INC.

Indirect flat panel x-ray detector
Primary Device ID60889978618132
NIH Device Record Keyaafb0f84-0d2a-4bd4-8b74-c1037e240af3
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRX Plus 2530 C Detector
Version Model NumberDRX Plus 2530 C Detector
Catalog Number8618134
Company DUNS793169512
Company NameCARESTREAM HEALTH, 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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS160889978618132 [Primary]

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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-23
Device Publish Date2020-07-15

On-Brand Devices [DRX Plus 2530 C Detector]

60889978618132DRX2530C DETECTOR /MOBILE
60889978618149DRX2530C DETECTOR /RETROFITS
60889978615247DRX PLUS 2530C DETECTOR/ MOBILE
60889978615179DRX PLUS 2530C DETECTOR/ EVOLUTION
60889978615148DRX PLUS 2530C DETECTOR/ RETROFIT

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