AnyRidge Int. Dummy (Marketing) M-DMFANIHX5510

GUDID 08809708759973

AnyRidge Internal Implant System

Megagen Implant Co. Ltd

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• Primary Device ID: 08809708759973
• NIH Device Record Key: 8fd46fbe-3b97-4cf0-9eae-75b6318eb22c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AnyRidge Int. Dummy (Marketing)
• Version Model Number: FANIHX5510
• Catalog Number: M-DMFANIHX5510
• Company DUNS: 687388178
• Company Name: Megagen Implant Co. Ltd
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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	08809708759973 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K122231

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: 2023-11-16
• Device Publish Date: 2023-11-08

On-Brand Devices [AnyRidge Int. Dummy (Marketing)]

• 08809708759980: AnyRidge Internal Implant System
• 08809708759973: AnyRidge Internal Implant System
• 08809708759966: AnyRidge Internal Implant System