BrightMatter Plan SYN-0004

GUDID 00670082000085

Synaptive Medical Inc

Radiology PACS software Radiology PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software Radiological PACS software
Primary Device ID00670082000085
NIH Device Record Keyc57d1cbc-8366-4590-97f9-d67c216521ad
Commercial Distribution Discontinuation2019-08-06
Commercial Distribution StatusNot in Commercial Distribution
Brand NameBrightMatter Plan
Version Model Number1.3
Catalog NumberSYN-0004
Company DUNS203061833
Company NameSynaptive Medical Inc
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100670082000085 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LLZSystem, Image Processing, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number7
Public Version Date2019-08-16
Device Publish Date2016-09-24

On-Brand Devices [BrightMatter Plan]

006700820004121.6
006700820003681.5
006700820001601.4
006700820000851.3
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.