Progeny imaging Domestic 500-427

GUDID 00841709105661

Progeny Imaging Software

MIDMARK CORPORATION

General-purpose dental x-ray system application software
Primary Device ID00841709105661
NIH Device Record Keyebff15f3-0e1e-41f6-a4da-1f1114bb7bd0
Commercial Distribution StatusIn Commercial Distribution
Brand NameProgeny imaging Domestic
Version Model Number500-427
Catalog Number500-427
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 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

Customer Support Contacts

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

Device Identifiers

Device Issuing AgencyDevice ID
GS100841709105661 [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 Date2016-11-04

Devices Manufactured by MIDMARK CORPORATION

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