Primary Device ID | 08714729202547 |
NIH Device Record Key | 304e8b0a-95bc-48cf-9220-66db06bee364 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guider Softip™ XF |
Version Model Number | H965100500 |
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 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729202547 [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 | 2020-07-23 |
Device Publish Date | 2016-09-24 |
08714729283553 | Guide Catheter |
08714729283546 | Guide Catheter |
08714729283539 | Guide Catheter |
08714729283522 | Guide Catheter |
08714729283515 | Guide Catheter |
08714729283508 | Guide Catheter |
08714729244394 | Guide Catheter |
08714729244387 | Guide Catheter |
08714729244370 | Guide Catheter |
08714729244356 | Guide Catheter |
08714729244349 | Guide Catheter |
08714729244332 | Guide Catheter |
08714729244318 | Guide Catheter |
08714729244301 | Guide Catheter |
08714729244295 | Guide Catheter |
08714729202561 | Guide Catheter |
08714729202554 | Guide Catheter |
08714729202547 | Guide Catheter |
08714729202523 | Guide Catheter |
08714729202516 | Guide Catheter |
08714729202509 | Guide Catheter |
08714729202486 | Guide Catheter |
08714729202479 | Guide Catheter |
08714729202462 | Guide Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUIDER SOFTIP 76330341 2800935 Live/Registered |
STRYKER CORPORATION 2001-10-25 |
GUIDER SOFTIP 76330341 2800935 Live/Registered |
STRYKER NV OPERATIONS LIMITED 2001-10-25 |