| Primary Device ID | 00842271158727 | 
| NIH Device Record Key | 5731e9f2-a0f9-4374-8c74-3bcfe41dad1c | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | NexxZr Plus Multi 2.0 D2 W98-20mm | 
| Version Model Number | 760393 | 
| 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 | 00842271158727 [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 | 
| 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 | 
| 00842271158727 - NexxZr Plus Multi 2.0 D2 W98-20mm | 2024-03-28 | 
| 00842271158734 - NexxZr Plus Multi 2.0 D3 W98-20mm | 2024-03-28 |