ET Multi Ti Base

GUDID 00810019244599

HIOSSEN, INC.

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• Primary Device ID: 00810019244599
• NIH Device Record Key: 5d7fd717-9529-4357-a46a-aba6636bc830
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ET Multi Ti Base
• Version Model Number: ETMTB0410G
• Company DUNS: 796083090
• Company Name: HIOSSEN, INC.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810019244599 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K182091

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-27
• Device Publish Date: 2021-09-17

On-Brand Devices [ET Multi Ti Base]

• 00810019244612: ETMTB0605G
• 00810019244605: ETMTB0605
• 00810019244599: ETMTB0410G
• 00810019244582: ETMTB0410
• 00810019244575: ETMTB0405G
• 00810019244568: ETMTB0405