Minerva PTA Balloon Dilatation Catheter 803-080005-150U

GUDID 06958481419610

BrosMed Medical Co.,Ltd.

Peripheral angioplasty balloon catheter, basic
Primary Device ID06958481419610
NIH Device Record Key2cfa1463-c847-44b4-aa34-063920899e73
Commercial Distribution StatusIn Commercial Distribution
Brand NameMinerva PTA Balloon Dilatation Catheter
Version Model Numberrev 01
Catalog Number803-080005-150U
Company DUNS421318800
Company NameBrosMed Medical Co.,Ltd.
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106958481419610 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LITCatheter, Angioplasty, Peripheral, Transluminal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-10-31

On-Brand Devices [Minerva PTA Balloon Dilatation Catheter]

06958481419962rev 01
06958481419955rev 01
06958481419948rev 01
06958481419931rev 01
06958481419924rev 01
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06958481419665rev 01
06958481419658rev 01
06958481419641rev 01
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06958481419610rev 01
06958481419603rev 01
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06958481419528rev 01
06958481419511rev 01
06958481419504rev 01
06958481419498rev 01
06958481419481rev 01
06958481419474rev 01

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