GUDID 07290108816853

Mono, D3.75, L16, Bendable One Piece Ti. Implant

NORIS MEDICAL LTD

Screw endosteal dental implant, one-piece
Primary Device ID07290108816853
NIH Device Record Key0ba4d144-757b-4aba-bb89-2cbe5f992573
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberNMBV3716
Company DUNS649340106
Company NameNORIS MEDICAL LTD
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
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
GS107290108816853 [Primary]
GS117290108816850 [Package]
Package: 5PACK [5 Units]
In Commercial Distribution

FDA Product Code

DZEImplant, Endosseous, Root-Form

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-01-22
Device Publish Date2017-11-20

Devices Manufactured by NORIS MEDICAL LTD

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07290116151557 - Tuff PRO Implant2025-04-04 Tuff PRO, D5.0, L13, Int. Hex Ti. Implant
07290116151564 - Tuff PRO Implant2025-04-04 Tuff PRO, D5.0, L16, Int. Hex Ti. Implant
07290116151571 - Tuff Implant2025-04-04 Tuff, D3.3, L8, Int. Hex Ti. Implant
07290116151588 - Tuff Implant2025-04-04 Tuff, D3.3, L10, Int. Hex Ti. Implant
07290116151397 - Tuff PRO Implant2025-04-02 Tuff PRO, D3.75, L13, Int. Hex Ti. Implant
07290116151403 - Tuff PRO Implant2025-04-02 Tuff PRO, D3.75, L16, Int. Hex Ti. Implant
07290116151427 - Tuff PRO Implant2025-04-02 Tuff PRO, D4.2, L8, Int. Hex Ti. Implant
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