Admira Fusion Flow 2821

GUDID E22128211

Flowable light-cured Nano-Hybrid Ormocer (ORganically-MOdified CERamic)

VOCO GmbH

Dental composite resin

• Primary Device ID: E22128211
• NIH Device Record Key: 25642961-3291-44a4-b806-6f9af057328f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Admira Fusion Flow
• Version Model Number: 2821
• Catalog Number: 2821
• Company DUNS: 316699578
• Company Name: VOCO GmbH
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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

Customer Support Contacts

• Phone: 999-999-9999
• Email: xxx@xx.xx

Operating and Storage Conditions

• Storage Environment Temperature: Between 4 Degrees Celsius and 23 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E22128211 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153177

FDA Product Code

• EBF: Material, Tooth Shade, Resin

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-07

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• E22128161: Flowable light-cured Nano-Hybrid Ormocer (ORganically-MOdified CERamic) Kit: 5 × 2 g syringes (