VITA STARTER KIT

GUDID J017EC4STKITS40

VITA STARTER KIT CAD/CAM BLOCKS (IV)

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

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• Primary Device ID: J017EC4STKITS40
• NIH Device Record Key: 6c27f325-7a83-4090-8433-42881fe26ea2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITA STARTER KIT
• Version Model Number: VITA STARTER KIT CAD/CAM BLOCKS (IV)
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J017EC4STKITS40 [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: 2024-06-28
• Device Publish Date: 2024-06-20

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

• J017EC4STKITS40 - VITA STARTER KIT: 2024-06-28VITA STARTER KIT CAD/CAM BLOCKS (IV)
• J017EC4STKITS40 - VITA STARTER KIT: 2024-06-28 VITA STARTER KIT CAD/CAM BLOCKS (IV)
• J017EDMYS79814440 - VITA YZ: 2024-06-28 VITA YZ® STMulticolor, B4, Ø 98.4 x h 14 mm, 1 pc.
• J017EDMYS79814480 - VITA YZ: 2024-06-28 VITA YZ® STMulticolor, C4, Ø 98.4 x h 14 mm, 1 pc.
• J017EDMYS79825400 - VITA YZ: 2024-06-28 VITA YZ® STMulticolor, A4, Ø 98.4 x h 25 mm, 1 pc.
• J017C44433F40 - VITAVM LC: 2024-06-26 VITA VM LC flow BASE DENTINE, A3, 4 g, ENL
• J017EDMYS79818430 - VITA YZ: 2024-06-26 VITA YZ® STMulticolor, B3, Ø 98.4 x h 18 mm, 1 pc.
• J017EDMYS79818440 - VITA YZ: 2024-06-26 VITA YZ® STMulticolor, B4, Ø 98.4 x h 18 mm, 1 pc.
• J017EDMYS79818510 - VITA YZ: 2024-06-26 VITA YZ® STMulticolor, D4, Ø 98.4 x h 18 mm, 1 pc.