VITABLOCS

GUDID J017EC41M2CTF120

VITABLOCS TriLuxe forte for CEREC/inLab 1M2C TF12 10 St.

Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft

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• Primary Device ID: J017EC41M2CTF120
• NIH Device Record Key: 3d52683c-8f5f-4c9f-9186-ac9e331205cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITABLOCS
• Version Model Number: EC41M2CTF12
• Company DUNS: 315165357
• Company Name: Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft
• 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: 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

Customer Support Contacts

• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J017EC41M2CTF120 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102128

FDA Product Code

• EIH: POWDER, PORCELAIN

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: 2021-04-27
• Device Publish Date: 2021-04-19

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• J017EC42M2CTF120: VITABLOCS TriLuxe forte for CEREC/inLab 2M2C TF12 10 St.
• J017EC41M2CTF120: VITABLOCS TriLuxe forte for CEREC/inLab 1M2C TF12 10 St.
• J017EC41M1CTF140: VITABLOCS TriLuxe forte for CEREC/inLab
• J017EC41M1CTF1250: VITABLOCS TriLuxe forte for CEREC/inLab
• J017EC40M1CTF140: VITABLOCS TriLuxe forte for CEREC/inLab
• J017EC40M1CTF1250: VITABLOCS TriLuxe forte for CEREC/inLab