Hybrid Link UNHL 40552H

GUDID 08800049278918

DIO Corporation

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 08800049278918
• NIH Device Record Key: 3d8e3bd1-47ee-46fa-a877-a25129d264e3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hybrid Link
• Version Model Number: UNHL 40552H
• Catalog Number: UNHL 40552H
• Company DUNS: 631085206
• Company Name: DIO Corporation
• 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: 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	08800049278918 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K181037

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[08800049278918]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-03-18
• Device Publish Date: 2020-03-10

On-Brand Devices [Hybrid Link]

• 08800049278925: UNHL 40553H
• 08800049278918: UNHL 40552H
• 08800049278901: UNHL 40551H
• 08800049278895: UNHL 40403H
• 08800049278888: UNHL 40402H
• 08800049278871: UNHL 40401H