Ti Base RP Abutment, RH 4mm GH 3mm Angular Engaged

GUDID 07290109306476

ADIN DENTAL IMPLANT SYSTEMS LTD

Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed Dental implant suprastructure, permanent, preformed

• Primary Device ID: 07290109306476
• NIH Device Record Key: f6e81ca4-70d2-4999-b166-226b814a946b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ti Base RP Abutment, RH 4mm GH 3mm Angular Engaged
• Version Model Number: TB03433
• Company DUNS: 533289435
• Company Name: ADIN DENTAL IMPLANT SYSTEMS LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109306476 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112585

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

[07290109306476]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-06-10
• Device Publish Date: 2021-06-02

Devices Manufactured by ADIN DENTAL IMPLANT SYSTEMS LTD

• 07290109308746 - NP Straight Single TMA 1mm: 2024-02-12
• 07290109308753 - NP Straight Single TMA 2mm: 2024-02-12
• 07290109308760 - NP Straight Single TMA 3mm: 2024-02-12
• 07290109308777 - NP Angled Single TMA 17° 3mm: 2024-02-12
• 07290109308784 - NP Angled Single TMA 30° 3.5mm: 2024-02-12
• 07290109308791 - NP Angled Single TMA 30° 5mm: 2024-02-12
• 07290109308807 - NP Angled Single TMA 17° 4mm: 2024-02-12
• 07290109308814 - NP Straight Single TMA 4mm: 2024-02-12