DRYPRO MODEL 832

GUDID 04560141921641

KONICA MINOLTA, INC.

Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera
Primary Device ID04560141921641
NIH Device Record Key105bd5eb-fad6-46aa-bd07-f169b3658272
Commercial Distribution StatusIn Commercial Distribution
Brand NameDRYPRO MODEL 832
Version Model NumberGM76
Company DUNS692076161
Company NameKONICA MINOLTA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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
GS104560141921641 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LMCCamera, Multi Format, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-10-29
Device Publish Date2016-09-19

On-Brand Devices [DRYPRO MODEL 832]

04560141922686GNPM
04560141921641GM76

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