Multi Post Screw AANMSF

GUDID 08806388202911

AnyRidge Internal M1.8

Megagen Implant Co. Ltd

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08806388202911
• NIH Device Record Key: 505f6ac8-15bd-4d81-aff8-1db35afe22d3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Multi Post Screw
• Version Model Number: AANMSF
• Catalog Number: AANMSF
• 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	08806388202911 [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

[08806388202911]

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 [Multi Post Screw]

• 08806388215430: ExFeel Internal M2
• 08806388202911: AnyRidge Internal M1.8
• 08806388202928: XPEED AnyRidge Internal Implant System M1.8
• 08809708752165: XPEED AnyRidge Internal Implant System M1.8
• 08809708752127: ExFeel Internal System M2