Primary Device ID | 08714729889786 |
NIH Device Record Key | 2bcd4caf-08b5-47d9-8677-24ed26de6a9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AngioJet® Distaflex™ |
Version Model Number | 111304-001 |
Catalog Number | 111304 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729889786 [Primary] |
MCX | CATHETER, CORONARY, ATHERECTOMY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-08-05 |
Device Publish Date | 2015-04-21 |
08714729269779 - Polaris X™ | 2025-02-04 Catheter Cable, Sterile Cable |
08714729839835 - Direxion™ HI-FLO™ Transend™-18 System | 2025-01-23 Pre-Loaded Torqueable Microcatheter |
08714729269915 - Electrophysiology Cable | 2025-01-15 Sterile Cable |
08714729877868 - Radia™ | 2025-01-08 Bidirectional Steerable Diagnostic Catheter |
08714729877875 - Radia™ | 2025-01-08 Bidirectional Steerable Diagnostic Catheter |
08714729877882 - Radia™ | 2025-01-08 Bidirectional Steerable Diagnostic Catheter |
08714729877899 - Radia™ | 2025-01-08 Bidirectional Steerable Diagnostic Catheter |
08714729877905 - Radia™ | 2025-01-08 Bidirectional Steerable Diagnostic Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ANGIOJET 74641870 1976193 Live/Registered |
BOSTON SCIENTIFIC LIMITED 1995-03-03 |