Ti Base UniFit Abutment, RH 4mm GH 3mm Angular Wide

GUDID 07290109304908

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

• Primary Device ID: 07290109304908
• NIH Device Record Key: f6a0b624-eda3-4565-ae8c-dc620fd998d6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ti Base UniFit Abutment, RH 4mm GH 3mm Angular Wide
• Version Model Number: TB07433W
• Company DUNS: 533289435
• Company Name: ADIN DENTAL IMPLANT SYSTEMS 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: 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	07290109304908 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223714

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

[07290109304908]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-12
• Device Publish Date: 2024-01-04

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• 07290109307824 - UniFit Star Torque Driver-Short: 2024-04-29
• 07290109307831 - UniFit Star Torque Driver-Long: 2024-04-29
• 07290109307848 - UniFit Ratchet Retrieval Tool for Abutments: 2024-04-29
• 07290116770284 - UniFit Ratchet Retrieval Tool: 2024-04-29
• 07290116770321 - Guided UniFit Ratchet Fixture Mount S-5.5: 2024-04-29
• 07290116770352 - Guided UniFit Ratchet Fixture Mount S-5.5, Screw Retained: 2024-04-29