3i 5.0mm Non-Hex Cylinder, .050"/1.25mm Hex Screw & Occlusal Plug 51-500252

GUDID 10841307118558

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 10841307118558
• NIH Device Record Key: 15e1f126-91e1-410d-9302-98973cadd45e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3i 5.0mm Non-Hex Cylinder, .050"/1.25mm Hex Screw & Occlusal Plug
• Version Model Number: 51-500252
• Catalog Number: 51-500252
• Company DUNS: 868856969
• Company Name: IMPLANT DIRECT SYBRON MANUFACTURING LLC
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 1-888-649-6425
• Email: customerservice@implantdirect.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841307118558 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K904236

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

[10841307118558]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-10-16

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