Tuff PRO Implant NM1F3308

GUDID 07290116151311

Screw endosteal dental implant, two-piece

Primary Device ID	07290116151311
NIH Device Record Key	0f11fec4-c16e-4d53-a44c-42961f2b12a2
Commercial Distribution Status	In Commercial Distribution
Brand Name	Tuff PRO Implant
Version Model Number	NM1F3308
Catalog Number	NM1F3308
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

Device Issuing Agency	Device ID
GS1	07290116151311 [Primary]

DZE	Implant, Endosseous, Root-Form

Steralize Prior To Use	false
Device Is Sterile	true

07290116151311 - Tuff PRO Implant	2025-02-12Tuff PRO, D3.3, L8, Int. Hex Ti. Implant
07290116151311 - Tuff PRO Implant	2025-02-12 Tuff PRO, D3.3, L8, Int. Hex Ti. Implant
07290108815580 - NA	2023-11-27 Mono, D5.0, L16, One Piece Ti. Implant
07290108816839 - NA	2020-01-22 Mono, D3.75,L11.5, Bendable One Piece Ti. Implant
07290108816846 - NA	2020-01-22 Mono, D3.75, L13, Bendable One Piece Ti. Implant
07290108816853 - NA	2020-01-22 Mono, D3.75, L16, Bendable One Piece Ti. Implant
07290108816860 - NA	2020-01-22 Mono, D4.2, L11.5, Bendable One Piece Ti.Implant
07290108816877 - NA	2020-01-22 Mono, D4.2, L13, Bendable One Piece Ti.Implant
07290108816884 - NA	2020-01-22 Mono, D4.2, L16, Bendable One Piece Ti. Implant