| Primary Device ID | 10190707088283 |
| NIH Device Record Key | 3d0cfc44-f29f-44a1-9c10-c916ae044578 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Carriere D-LX |
| Version Model Number | 103-192C |
| Company DUNS | 062165188 |
| Company Name | ORTHO ORGANIZERS, INC. |
| Device Count | 10 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00190707088286 [Primary] |
| GS1 | 10190707088283 [Unit of Use] |
| ECN | CLAMP, WIRE, ORTHODONTIC |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-26 |
| Device Publish Date | 2025-06-18 |
| 10190707088498 | 019x025 Carriere D-LX CuNitanium 35° w/ EZ Stops Single Pack(10) |
| 10190707088467 | 017x025 Carriere D-LX CuNitanium 35° w/ EZ Stops Single Pack(10) |
| 10190707088351 | 014x025 Carriere D-LX CuNitanium 27° w/ EZ Stops Single Pack(10) |
| 10190707088283 | 014 Carriere D-LX Cu Nitanium 27° w/ EZ Stops Single Pack (10) |
| 10190707088252 | 013 Carriere D-LX Cu Nitanium 27° w/ EZ Stops Single Pack (10) |