GUDID 06009544016250

Internal Octagon Implant, Ø6.5 Platform, Maxit™, Ø8.0 x 11mm

SOUTHERN IMPLANTS (PTY) LTD

Screw endosteal dental implant, two-piece

• Primary Device ID: 06009544016250
• NIH Device Record Key: 4c37d009-6da5-4d61-89cc-ef04074c5b72
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: MAXIT8-11F
• Company DUNS: 636239584
• Company Name: SOUTHERN IMPLANTS (PTY) 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: false
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	06009544016250 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071161

FDA Product Code

• DZE: Implant, Endosseous, Root-Form

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-02-11
• Device Publish Date: 2019-01-10

Devices Manufactured by SOUTHERN IMPLANTS (PTY) LTD

• 06009544038252 - NA: 2024-11-06 Screw Ti Hex Series L3.5mm
• 06009544039952 - N/A: 2024-11-01 Screw Titanium Hex 1 Series ø2.7 Head
• 06009544039969 - N/A: 2024-11-01 Screw Ti Hexed M1.4 NLT
• 06009544048589 - N/A: 2024-09-03 Implant SP1 Ø4.0x10mm
• 06009544048596 - N/A: 2024-09-03 Implant SP1 Ø4.0x11mm
• 06009544048619 - N/A: 2024-09-03 Implant SP1 Ø4.0x15mm
• 06009544048626 - N/A: 2024-09-03 Implant SP1 Ø4.0x18mm
• 06009544048633 - N/A: 2024-09-03 Implant SP1 Ø4.0x20mm