| Primary Device ID | 05055662929317 |
| NIH Device Record Key | ac6e50db-e056-4a73-8056-888fa99d3710 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ORTHO SOLUTIONS EXTREMITY FIXATION IMPLANTS FOR OSTEOSYSNTHESIS |
| Version Model Number | OS310907 |
| Catalog Number | OS310907 |
| Company DUNS | 218648211 |
| Company Name | ORTHO SOLUTIONS HOLDINGS LIMITED |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Phone | +441621843599 |
| quality@orthosol.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05055662929317 [Primary] |
| HRS | Plate, Fixation, Bone |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[05055662929317]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-04-06 |
| Device Publish Date | 2016-05-16 |
| 05055662929355 | EFS DRILL GUIDE 2.4MM/3.0MM SCREW |
| 05055662929348 | EFS DRILL GUIDE 1.2MM/2.0MM SCREW |
| 05055662929317 | COMPRESSION STAPLE DRILL GUIDE 2.7MM |
| 05055662929294 | MEMO STAPLE UNIVERSAL SPREADER |
| 05055662929287 | MEMO STAPLE 20MM & 25MM & 16MM EXPANDER |
| 05055662929270 | MEMO STAPLE 10MM & 12MM EXPANDER |
| 05055662928921 | FOS DRILL GUIDE |
| 05055662923780 | FPS 2.7MM DRILL GUIDE SHORT |