Primary Device ID | 08714729308218 |
NIH Device Record Key | 1230b4ff-b823-437f-a93e-b3e96597e61b |
Commercial Distribution Discontinuation | 2018-12-21 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Wiseguide™ |
Version Model Number | H749195004470 |
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 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729308218 [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 |
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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 |