VITA Interno BISETV3

GUDID J017BISETV30

VITA INTERNO KIT

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

Dental appliance fabrication material, ceramic

• Primary Device ID: J017BISETV30
• NIH Device Record Key: abaa3fa1-b4e4-4909-9d86-78f8798ccec9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VITA Interno
• Version Model Number: BISETV3
• Catalog Number: BISETV3
• 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: 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: +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
• Phone: +1(800)8283839
• Email: info@vitanorthamerica.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J017BISETV30 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K901982

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: 2021-11-08
• Device Publish Date: 2021-10-29

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

• J017EC4YM80278040 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-20/19, 0M1, 4 pcs.
• J017EC4YM80279220 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-44/19, 0M1, 2 pcs.
• J017EC4YM83678040 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-20/19, A1, 4 pcs.
• J017EC4YM83679220 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-44/19, A1, 2 pcs.
• J017EC4YM83778040 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-20/19, A2, 4 pcs.
• J017EC4YM83779220 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-44/19, A2, 2 pcs.
• J017EC4YM83878040 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-20/19, A3, 4 pcs.
• J017EC4YM83879220 - VITA YZ MULTI TRANSLUCENT: 2025-03-18 VITA YZ MULTI TRANSLUCENT for CEREC, YZ-44/19, A3, 2 pcs.