Primary Device ID | 08714729042549 |
NIH Device Record Key | af730cf0-fbb4-4f06-9165-0b50ace15551 |
Commercial Distribution Discontinuation | 2023-05-11 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Passport |
Version Model Number | M0062181010 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 08714729042549 [Primary] |
EZN | DILATOR, CATHETER, URETERAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-04-05 |
Device Publish Date | 2016-09-24 |
08714729191872 | Balloon Dilatation Catheter |
08714729154969 | Balloon Dilatation Catheter |
08714729154921 | Balloon Dilatation Catheter |
08714729042549 | Balloon Dilatation Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PASSPORT 98747634 not registered Live/Pending |
GroPro Corporation 2024-09-12 |
PASSPORT 98669203 not registered Live/Pending |
Beyond Earth, LLC 2024-07-26 |
PASSPORT 98176230 not registered Live/Pending |
Amazon Technologies, Inc. 2023-09-12 |
PASSPORT 98087314 not registered Live/Pending |
Passport, Inc. 2023-07-17 |
PASSPORT 98045988 not registered Live/Pending |
777ABC, LLC 2023-06-16 |
PASSPORT 98028348 not registered Live/Pending |
Circonus, Inc. 2023-06-05 |
PASSPORT 98028171 not registered Live/Pending |
CNA Financial Corporation 2023-06-05 |
PASSPORT 97792011 not registered Live/Pending |
Crewfare LLC 2023-02-13 |
PASSPORT 97607747 not registered Live/Pending |
MillerKnoll, Inc. 2022-09-26 |
PASSPORT 97551854 not registered Live/Pending |
Pelco Products, Inc. 2022-08-17 |
PASSPORT 97470517 not registered Live/Pending |
ProviderTrust, Inc. 2022-06-22 |
PASSPORT 97457298 not registered Live/Pending |
Baylis Medical Technologies Inc. 2022-06-14 |