| Primary Device ID | 00810129551723 |
| NIH Device Record Key | 204e44b5-4b13-4897-ad8b-1c3900a2a275 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OvertureTi |
| Version Model Number | PKG-90-OSP-101730 |
| Company DUNS | 119105665 |
| Company Name | Overture Orthopaedics |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Width | 17.5 Millimeter |
| Length | 30 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00810129551723 [Primary] |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-24 |
| Device Publish Date | 2025-03-14 |