GUDID 06009544008828

Healing Abutment for Ø5.0 DC, Ø6.5 x 4mm

SOUTHERN IMPLANTS (PTY) LTD

Dental implant suprastructure, temporary, preformed, single-use

• Primary Device ID: 06009544008828
• NIH Device Record Key: 5cca76d5-e8a9-48fa-95b6-fef7dc3aedaf
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: HA-DC5-W4
• 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	06009544008828 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163060

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

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: 2019-02-07
• Device Publish Date: 2019-01-07

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