visio.lign system VO1G3A10

GUDID VO1G3A10

novo.lign P veneer posterior 1G3 upper A10 4 parts (14,15,16,17) 1 Assortment

bredent GmbH & Co. KG

Dental veneer, professional

• Primary Device ID: VO1G3A10
• NIH Device Record Key: e01df5bc-7ef1-46db-9e34-10259ad2fff3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: visio.lign system
• Version Model Number: novo.lign
• Catalog Number: VO1G3A10
• Company DUNS: 341086190
• Company Name: bredent GmbH & Co. KG
• 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: false
• Manufacturing Date: false
• 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: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com
• Phone: +4973098720
• Email: info@bredent.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry
• Special Storage Condition, Specify: Between 0 and 0 *dry

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	VO1G3A10 [Primary]

FDA Product Code

• ELM: Denture, Plastic, Teeth

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: 2021-02-05
• Device Publish Date: 2016-07-06

Devices Manufactured by bredent GmbH & Co. KG

• EBREVLCOLBLACK9 - visio.lign color Black: 2025-03-18 visio.lign color Black 2.6 ml
• EBREVLCOLBLUE9 - visio.lign color Blue: 2025-03-18 visio.lign color Blue 2.6 ml
• EBREVLCOLBODYA9 - visio.lign color Body A: 2025-03-18 visio.lign color Body A 2.6 ml
• EBREVLCOLBODYB9 - visio.lign color Body B: 2025-03-18 visio.lign color Body B 2.6 ml
• EBREVLCOLBODYC9 - visio.lign color Body C: 2025-03-18 visio.lign color Body C 2.6 ml
• EBREVLCOLBODYD9 - visio.lign color Body D: 2025-03-18 visio.lign color Body D 2.6 ml
• EBREVLCOLBROWN9 - visio.lign color Brown: 2025-03-18 visio.lign color Brown 2.6 ml
• EBREVLCOLCREME9 - visio.lign color Creme: 2025-03-18 visio.lign color Creme 2.6 ml