Tuff Implant NM2F3308

GUDID 07290116151571

Tuff, D3.3, L8, Int. Hex Ti. Implant

NORIS MEDICAL LTD

Screw endosteal dental implant, two-piece
Primary Device ID07290116151571
NIH Device Record Key7e17aa6c-0d76-4c28-a396-60fdf949f2d9
Commercial Distribution StatusIn Commercial Distribution
Brand NameTuff Implant
Version Model NumberNM2F3308
Catalog NumberNM2F3308
Company DUNS649340106
Company NameNORIS MEDICAL LTD
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com
Phone+972737964477
Emailinfo@norismedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107290116151571 [Primary]

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-04-04
Device Publish Date2025-03-27

On-Brand Devices [Tuff Implant]

07290116151588Tuff, D3.3, L10, Int. Hex Ti. Implant
07290116151571Tuff, D3.3, L8, Int. Hex Ti. Implant

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