Passport Kit

GUDID 08714729042594

Balloon Dilatation Catheter Kit

BOSTON SCIENTIFIC CORPORATION

Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated Urethral dilatation catheter, non-medicated
Primary Device ID08714729042594
NIH Device Record Keyc4584e53-ce6a-436e-a468-92ca1442bf61
Commercial Distribution Discontinuation2023-04-30
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePassport Kit
Version Model NumberM0062181300
Company DUNS021717889
Company NameBOSTON SCIENTIFIC CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS108714729042594 [Primary]

FDA Product Code

EZNDILATOR, CATHETER, URETERAL

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-04-05
Device Publish Date2016-09-24

On-Brand Devices [Passport Kit]

08714729042600Balloon Dilatation Catheter Kit
08714729042594Balloon Dilatation Catheter Kit
08714729042587Balloon Dilatation Catheter Kit
08714729042570Balloon Dilatation Catheter Kit

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.