| Primary Device ID | 00842271158673 |
| NIH Device Record Key | 495b3ef9-97c3-4df5-ad33-e469230eb91a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NexxZr Plus Multi 2.0 B4 W98-20mm |
| Version Model Number | 760388 |
| Company DUNS | 002265727 |
| Company Name | SAGEMAX BIOCERAMICS, INC |
| 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 | true |
| Expiration Date | false |
| 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 | 00842271158673 [Primary] |
| EIH | Powder, Porcelain |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-03-28 |
| Device Publish Date | 2024-03-20 |
| 00842271158666 - NexxZr Plus Multi 2.0 B3 W98-20mm | 2024-03-28 |
| 00842271158673 - NexxZr Plus Multi 2.0 B4 W98-20mm | 2024-03-28 |
| 00842271158673 - NexxZr Plus Multi 2.0 B4 W98-20mm | 2024-03-28 |
| 00842271158680 - NexxZr Plus Multi 2.0 C1 W98-20mm | 2024-03-28 |
| 00842271158697 - NexxZr Plus Multi 2.0 C2 W98-20mm | 2024-03-28 |
| 00842271158703 - NexxZr Plus Multi 2.0 C3 W98-20mm | 2024-03-28 |
| 00842271158710 - NexxZr Plus Multi 2.0 C4 W98-20mm | 2024-03-28 |
| 00842271158727 - NexxZr Plus Multi 2.0 D2 W98-20mm | 2024-03-28 |
| 00842271158734 - NexxZr Plus Multi 2.0 D3 W98-20mm | 2024-03-28 |