| 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 |
| 00191506060091 - OverStitch™ | 2025-09-29 Intragastric Balloon System |
| 08714729878018 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878025 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878049 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878056 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878063 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878070 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
| 08714729878087 - Viking™ | 2025-09-08 Fixed Curve Diagnostic Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CINCHPAD 77284962 3667255 Live/Registered |
ENDOCHOICE, INC. 2007-09-20 |