Hermes NC PTA Balloon Dilatation Catheter 820-090040-070U

GUDID 06958481449457

BrosMed Medical Co.,Ltd.

Peripheral angioplasty balloon catheter, basic
Primary Device ID06958481449457
NIH Device Record Key80ca03cb-9405-4a50-8f5b-9d56eb5a3e3e
Commercial Distribution StatusIn Commercial Distribution
Brand NameHermes NC PTA Balloon Dilatation Catheter
Version Model Numberrev 01
Catalog Number820-090040-070U
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
GS106958481449457 [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 Date2017-06-30

On-Brand Devices [Hermes NC PTA Balloon Dilatation Catheter]

06958481451566rev 01
06958481451559rev 01
06958481451542rev 01
06958481451535rev 01
06958481451528rev 01
06958481451511rev 01
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06958481451498rev 01
06958481451481rev 01
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06958481451290rev 01
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06958481451252rev 01
06958481451245rev 01
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06958481451207rev 01
06958481451191rev 01
06958481451184rev 01
06958481451177rev 01
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06958481451139rev 01
06958481451122rev 01
06958481451115rev 01
06958481451108rev 01
06958481451092rev 01
06958481451085rev 01
06958481451078rev 01

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