GUDID 07290108816877

Mono, D4.2, L13, Bendable One Piece Ti.Implant

NORIS MEDICAL LTD

Screw endosteal dental implant, one-piece

• Primary Device ID: 07290108816877
• NIH Device Record Key: f33890d4-580a-4a2b-bb91-07a778e7cb05
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: NMBV4213
• 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

Customer Support Contacts

• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com
• Phone: +972737964477
• Email: info@norismedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290108816877 [Primary]
GS1	17290108816874 [Package]; Package: 5PACK [5 Units]; In Commercial Distribution

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-22
• Device Publish Date: 2017-11-20

Devices Manufactured by NORIS MEDICAL LTD

• 07290116151540 - Tuff PRO Implant: 2025-04-04 Tuff PRO, D5.0, L11.5, Int. Hex Ti. Implant
• 07290116151557 - Tuff PRO Implant: 2025-04-04 Tuff PRO, D5.0, L13, Int. Hex Ti. Implant
• 07290116151564 - Tuff PRO Implant: 2025-04-04 Tuff PRO, D5.0, L16, Int. Hex Ti. Implant
• 07290116151571 - Tuff Implant: 2025-04-04 Tuff, D3.3, L8, Int. Hex Ti. Implant
• 07290116151588 - Tuff Implant: 2025-04-04 Tuff, D3.3, L10, Int. Hex Ti. Implant
• 07290116151397 - Tuff PRO Implant: 2025-04-02 Tuff PRO, D3.75, L13, Int. Hex Ti. Implant
• 07290116151403 - Tuff PRO Implant: 2025-04-02 Tuff PRO, D3.75, L16, Int. Hex Ti. Implant
• 07290116151427 - Tuff PRO Implant: 2025-04-02 Tuff PRO, D4.2, L8, Int. Hex Ti. Implant