| Primary Device ID | 08714729307808 |
| NIH Device Record Key | 67aa0457-3eb7-4257-b350-4be8abcccb2c |
| Commercial Distribution Discontinuation | 2018-12-21 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Wiseguide™ |
| Version Model Number | H74919500270 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729307808 [Primary] |
| DQY | CATHETER, PERCUTANEOUS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-01 |
| Device Publish Date | 2016-09-24 |
| 08714729833307 | Guide Catheter |
| 08714729309703 | Guide Catheter |
| 08714729309697 | Guide Catheter |
| 08714729309666 | Guide Catheter |
| 08714729309659 | Guide Catheter |
| 08714729309635 | Guide Catheter |
| 08714729309598 | Guide Catheter |
| 08714729309550 | Guide Catheter |
| 08714729309536 | Guide Catheter |
| 08714729309512 | Guide Catheter |
| 08714729309482 | Guide Catheter |
| 08714729308997 | Guide Catheter |
| 08714729308973 | Guide Catheter |
| 08714729308935 | Guide Catheter |
| 08714729308898 | Guide Catheter |
| 08714729308461 | Guide Catheter |
| 08714729308430 | Guide Catheter |
| 08714729308416 | Guide Catheter |
| 08714729308379 | Guide Catheter |
| 08714729308362 | Guide Catheter |
| 08714729308355 | Guide Catheter |
| 08714729308324 | Guide Catheter |
| 08714729308249 | Guide Catheter |
| 08714729308232 | Guide Catheter |
| 08714729308218 | Guide Catheter |
| 08714729308034 | Guide Catheter |
| 08714729308027 | Guide Catheter |
| 08714729308010 | Guide Catheter |
| 08714729307990 | Guide Catheter |
| 08714729307983 | Guide Catheter |
| 08714729307976 | Guide Catheter |
| 08714729307969 | Guide Catheter |
| 08714729307938 | Guide Catheter |
| 08714729307914 | Guide Catheter |
| 08714729307907 | Guide Catheter |
| 08714729307884 | Guide Catheter |
| 08714729307853 | Guide Catheter |
| 08714729307846 | Guide Catheter |
| 08714729307808 | Guide Catheter |
| 08714729307709 | Guide Catheter |
| 08714729307648 | Guide Catheter |
| 08714729307631 | Guide Catheter |
| 08714729307518 | Guide Catheter |
| 08714729307488 | Guide Catheter |
| 08714729307389 | Guide Catheter |
| 08714729307372 | Guide Catheter |
| 08714729307365 | Guide Catheter |
| 08714729307310 | Guide Catheter |
| 08714729307273 | Guide Catheter |
| 08714729307242 | Guide Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WISEGUIDE 88370995 not registered Live/Pending |
Effective Learning Systems LLC 2019-04-04 |
![]() WISEGUIDE 78275603 2903313 Dead/Cancelled |
Powell, Don R. 2003-07-17 |
![]() WISEGUIDE 75249123 2441210 Live/Registered |
BOSTON SCIENTIFIC SCIMED, INC. 1997-02-27 |
![]() WISEGUIDE 75237304 2242388 Dead/Cancelled |
DOTONE CORPORATION 1997-02-06 |