Midmark Progeny Imaging Software 45-A0023

GUDID 00841709101380

X-ray system application software

MIDMARK CORPORATION

General-purpose dental x-ray system application software
Primary Device ID00841709101380
NIH Device Record Keyb3ca5b76-c95b-4b95-b3e9-fb32a2d5b78d
Commercial Distribution StatusIn Commercial Distribution
Brand NameMidmark Progeny Imaging Software
Version Model Number45-A0023
Catalog Number45-A0023
Company DUNS005036025
Company NameMIDMARK CORPORATION
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-643-6275
Emailimagingtechsupport@midmark.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100841709101380 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MUHSystem,X-Ray,Extraoral Source,Digital

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 [Midmark Progeny Imaging Software]

00841709101410X-ray system application software
00841709101403X-ray system application software
00841709101397X-ray system application software
00841709101380X-ray system application software
00841709101373X-ray system application software

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