AeroDR P-12

GUDID 04560141941434

KONICA MINOLTA, INC.

Indirect flat panel x-ray detector
Primary Device ID04560141941434
NIH Device Record Keyb3b1efbc-62ae-4805-8d7b-2e2e6e4c8f78
Commercial Distribution StatusIn Commercial Distribution
Brand NameAeroDR P-12
Version Model NumberA85U
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

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104560141941434 [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 Number5
Public Version Date2019-05-07
Device Publish Date2016-09-19

On-Brand Devices [AeroDR P-12]

04560141941434A85U
04560141934399A50D

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