Tuff PRO Implant NM1F3313

GUDID 07290116151342

Tuff PRO, D3.3, L13, Int. Hex Ti. Implant

NORIS MEDICAL LTD

Screw endosteal dental implant, two-piece

• Primary Device ID: 07290116151342
• NIH Device Record Key: d65d0669-21c8-48ec-8df4-a7a9bcbecfb1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tuff PRO Implant
• Version Model Number: NM1F3313
• Catalog Number: NM1F3313
• 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290116151342 [Primary]

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-01
• Device Publish Date: 2025-03-24

On-Brand Devices [Tuff PRO Implant]

• 07290116151311: Tuff PRO, D3.3, L8, Int. Hex Ti. Implant
• 07290116151380: Tuff PRO, D3.75, L11.5, Int. Hex Ti. Implant
• 07290116151373: Tuff PRO, D3.75, L10, Int. Hex Ti. Implant
• 07290116151366: Tuff PRO, D3.75, L8, Int. Hex Ti. Implant
• 07290116151359: Tuff PRO, D3.3, L16, Int. Hex Ti. Implant
• 07290116151342: Tuff PRO, D3.3, L13, Int. Hex Ti. Implant
• 07290116151335: Tuff PRO, D3.3, L11.5, Int. Hex Ti. Implant
• 07290116151328: Tuff PRO, D3.3, L10, Int. Hex Ti. Implant
• 07290116151533: Tuff PRO, D5.0, L10, Int. Hex Ti. Implant
• 07290116151526: NM1F5008
• 07290116151465: Tuff PRO, D4.2, L16, Int. Hex Ti. Implant
• 07290116151458: Tuff PRO, D4.2, L13, Int. Hex Ti. Implant
• 07290116151441: Tuff PRO, D4.2, L11.5, Int. Hex Ti. Implant
• 07290116151434: Tuff PRO, D4.2, L10, Int. Hex Ti. Implant
• 07290116151427: Tuff PRO, D4.2, L8, Int. Hex Ti. Implant
• 07290116151403: Tuff PRO, D3.75, L16, Int. Hex Ti. Implant
• 07290116151397: Tuff PRO, D3.75, L13, Int. Hex Ti. Implant
• 07290116151564: Tuff PRO, D5.0, L16, Int. Hex Ti. Implant
• 07290116151557: Tuff PRO, D5.0, L13, Int. Hex Ti. Implant
• 07290116151540: Tuff PRO, D5.0, L11.5, Int. Hex Ti. Implant
• 07290108817638: Tuff PRO, D5.0, L8, Int. Hex Ti. Implant
• 07290108817621: Tuff PRO, D4.2, L8, Int. Hex Ti. Implant
• 07290108817614: Tuff PRO, D3.75, L8, Int. Hex Ti. Implant
• 07290108817607: Tuff PRO, D3.3, L8, Int. Hex Ti. Implant