GUDID 08714729035886

Torque Vise

BOSTON SCIENTIFIC CORPORATION

Torque manipulation device
Primary Device ID08714729035886
NIH Device Record Keyffb4fcd4-2078-4446-8ea6-e06239e0c98e
Commercial Distribution Discontinuation2023-02-07
Commercial Distribution StatusNot in Commercial Distribution
Version Model NumberM001465500
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 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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108714729035886 [Package]
Contains: 08714729741404
Package: [12 Units]
Discontinued: 2023-02-07
Not in Commercial Distribution
GS108714729741404 [Primary]

FDA Product Code

OCYEndoscopic guidewire, gastroenterology-urology

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2025-03-11
Device Publish Date2016-09-24

Devices Manufactured by BOSTON SCIENTIFIC CORPORATION

00191506044466 - WallFlex™2025-03-11 Stent System
00191506044473 - WallFlex™2025-03-11 Stent System
00191506044480 - WallFlex™2025-03-11 Stent System
00191506044497 - WallFlex™2025-03-11 Stent System
00191506044503 - WallFlex™2025-03-11 Stent System
00191506044510 - WallFlex™2025-03-11 Stent System
00191506044527 - WallFlex™2025-03-11 Stent System
08714729035886 - NA2025-03-11Torque Vise
08714729035886 - NA2025-03-11 Torque Vise

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.