| Primary Device ID | 10871321001833 |
| NIH Device Record Key | 4e4d9708-b95f-4b86-9d6f-5c408417f0cb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Boat |
| Version Model Number | S 3012 |
| Company DUNS | 248911026 |
| Company Name | Labtician Ophthalmics, Inc |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00871321001836 [Unit of Use] |
| GS1 | 10871321001833 [Primary] |
| HQJ | Implant, Absorbable, (Scleral Buckling Methods) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2021-01-28 |
| Device Publish Date | 2015-10-09 |
| 18713210001833 | S 3012 |
| 18713210001826 | S 3012 |
| 18713210001680 | S 2989 |
| 10871321001833 | S 3012 |
| 10871321001826 | S 3012 |
| 10871321001680 | S 2989 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BOAT 87821754 5580285 Live/Registered |
Carton Brewing Company, LLC 2018-03-06 |
![]() BOAT 87190035 5353247 Live/Registered |
BEARD INTERNATIONAL SERVICES AND TECHNOLOGIES, L.L.C. 2016-09-30 |
![]() BOAT 85450899 4377112 Live/Registered |
Manring, Chris 2011-10-19 |
![]() BOAT 78187416 2850751 Live/Registered |
KALKOMEY ENTERPRISES, LLC 2002-11-21 |
![]() BOAT 73807671 1605175 Dead/Cancelled |
DIAMANDIS COMMUNICATIONS INC. 1989-06-19 |
![]() BOAT 73641013 1455138 Dead/Cancelled |
UNITED INDUSTRIES, INC. 1987-01-23 |