REGIUS Cassette/Plate

GUDID 04560141930957

KONICA MINOLTA, INC.

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Primary Device ID04560141930957
NIH Device Record Key9be9fc4e-d656-4d3e-b5fb-458147763e28
Commercial Distribution StatusIn Commercial Distribution
Brand NameREGIUS Cassette/Plate
Version Model NumberKCWQ
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 Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS104560141930957 [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 Date2016-09-19

On-Brand Devices [REGIUS Cassette/Plate]

04560141930964KCU5
04560141930957KCWQ
04560141930940KC6G
04560141930933KCTC
04560141930926KCSK
04560141930919KCQ0
04560141930902KCMM
04560141926141JFJ8
04560141925472BUN2
04560141922792KCLU
04560141922747KCPJ
04560141922730KCKD

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