Fuse Abutment AANTAH5012T

GUDID 08806388204243

AnyRidge Internal Ø5/ Hex/ Milling

Megagen Implant Co. Ltd

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08806388204243
• NIH Device Record Key: 097d4739-50cb-4643-983d-9763c858708f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fuse Abutment
• Version Model Number: AANTAH5012
• Catalog Number: AANTAH5012T
• Company DUNS: 687388178
• Company Name: Megagen Implant Co. 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: true
• 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	08806388204243 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110955

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08806388204243]

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: 2015-06-24

On-Brand Devices [Fuse Abutment]

• 08806388204243: AnyRidge Internal Ø5/ Hex/ Milling
• 08806388208500: AnyOne Internal Implant System