Atropos PTA Balloon Dilatation Catheter 819-080030-090U

GUDID 06958481447477

BrosMed Medical Co.,Ltd.

Peripheral angioplasty balloon catheter, basic
Primary Device ID06958481447477
NIH Device Record Keybe413a9a-3a5b-41fe-8a4d-044407a5aba0
Commercial Distribution StatusIn Commercial Distribution
Brand NameAtropos PTA Balloon Dilatation Catheter
Version Model Numberrev 01
Catalog Number819-080030-090U
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
GS106958481447477 [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 Date2016-11-28

On-Brand Devices [Atropos PTA Balloon Dilatation Catheter]

06958481448726rev 01
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06958481448238rev 01

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