| Primary Device ID | 05420028754382 |
| NIH Device Record Key | 7a7b58d6-4a00-48ca-a6f3-bf4263eba6f6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Orfit Industries |
| Version Model Number | 33787/16MI/12MI+N |
| Company DUNS | 283679900 |
| Company Name | Orfit Industries NV |
| Device Count | 1 |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com | |
| Phone | +3233262026 |
| welcome@orfit.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05420028754382 [Primary] |
| IYE | Accelerator, linear, 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 | 2022-11-25 |
| Device Publish Date | 2022-11-17 |