| Primary Device ID | 07290108810363 |
| NIH Device Record Key | 1e6ee8b7-8292-48c1-9f23-3960a272b774 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | NM-A5709 |
| Company DUNS | 649340106 |
| Company Name | NORIS MEDICAL LTD |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +972737964477 |
| info@norismedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290108810363 [Primary] |
| NHA | Abutment, Implant, Dental, Endosseous |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07290108810363]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2017-07-15 |
| 07290108815580 - NA | 2023-11-27 Mono, D5.0, L16, One Piece Ti. Implant |
| 07290108816839 - NA | 2020-01-22 Mono, D3.75,L11.5, Bendable One Piece Ti. Implant |
| 07290108816846 - NA | 2020-01-22 Mono, D3.75, L13, Bendable One Piece Ti. Implant |
| 07290108816853 - NA | 2020-01-22 Mono, D3.75, L16, Bendable One Piece Ti. Implant |
| 07290108816860 - NA | 2020-01-22 Mono, D4.2, L11.5, Bendable One Piece Ti.Implant |
| 07290108816877 - NA | 2020-01-22 Mono, D4.2, L13, Bendable One Piece Ti.Implant |
| 07290108816884 - NA | 2020-01-22 Mono, D4.2, L16, Bendable One Piece Ti. Implant |
| 07290108810011 - NA | 2019-11-08 Angular Anatomic Abutment, Angle 15˚, Height 8.5mm, Shoulder 0.8mm, Ti. |