Angled MU abutment

GUDID 07290112280756

Angled MU abutment

DENTACK IMPLANTS LTD

Screw endosteal dental implant, two-piece

• Primary Device ID: 07290112280756
• NIH Device Record Key: 41ee885c-5511-4a0d-a634-71a3c5cb84da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Angled MU abutment
• Version Model Number: MU-1730
• Company DUNS: 514897185
• Company Name: DENTACK IMPLANTS 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

Customer Support Contacts

• Phone: +97297660379
• Email: info@pyramidion-is.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290112280756 [Primary]

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[07290112280756]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-03-11
• Device Publish Date: 2019-02-27

On-Brand Devices [Angled MU abutment ]

• 07290112280756: Angled MU abutment
• 07290112280732: Angled MU abutment 17-1.5