Primary Device ID | 07290116151571 |
NIH Device Record Key | 7e17aa6c-0d76-4c28-a396-60fdf949f2d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tuff Implant |
Version Model Number | NM2F3308 |
Catalog Number | NM2F3308 |
Company DUNS | 649340106 |
Company Name | NORIS MEDICAL LTD |
Device Count | 1 |
DM Exempt | false |
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 | true |
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 | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com | |
Phone | +972737964477 |
info@norismedical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290116151571 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-04 |
Device Publish Date | 2025-03-27 |
07290116151588 | Tuff, D3.3, L10, Int. Hex Ti. Implant |
07290116151571 | Tuff, D3.3, L8, Int. Hex Ti. Implant |