Primary Device ID | 00816849010045 |
NIH Device Record Key | f14591c7-087f-4a73-a48a-cb82f54852ff |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CinchPad™ |
Version Model Number | SPX-017-25 |
Catalog Number | SPX-017-25 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
Device Count | 25 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Expiration Date | false |
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 | 00816849010045 [Primary] |
GS1 | 08714729989561 [Unit of Use] |
KME | BEDDING, DISPOSABLE, MEDICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-11 |
Device Publish Date | 2019-01-11 |
00191506046330 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046347 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046354 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046361 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046378 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046385 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046392 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046408 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CINCHPAD 77284962 3667255 Live/Registered |
ENDOCHOICE, INC. 2007-09-20 |