| Primary Device ID | 00816849010014 |
| NIH Device Record Key | 7701de39-d7c2-44bd-b48a-f1f878559bc8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Auto-Band® |
| Version Model Number | DBL-293 |
| Company DUNS | 014154279 |
| Company Name | ENDOCHOICE, INC. |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com | |
| Phone | 888-632-3636 |
| customercare@endochoice.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00816849010014 [Primary] |
| MND | Ligator, Esophageal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-06-21 |
| Device Publish Date | 2016-09-08 |
| 00816849010038 | Ligator Assembly & Band Barrel w/7 non-Latex Bands |
| 00816849010021 | Ligator Assembly & Band Barrel w/7 Latex Bands |
| 00816849010014 | Ligator Assembly & Band Barrel w/7 Latex Bands |
| 00816849010007 | Ligator Assembly & Band Barrel w/7 non-Latex Bands |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AUTO-BAND 78148438 not registered Dead/Abandoned |
Texas Instruments Incorporated 2002-07-29 |