Primary Device ID | 07290108816860 |
NIH Device Record Key | abf39278-8789-4e93-886e-0d85c86a573c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | NMBV4211 |
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 | true |
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 | 07290108816860 [Primary] |
GS1 | 17290108816867 [Package] Package: 5PACK [5 Units] In Commercial Distribution |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-01-22 |
Device Publish Date | 2017-11-20 |
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 | 2020-01-22Mono, D4.2, L11.5, 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. |