VeneerNow Injectable Matrix System 9069336

GUDID 7290019259336

6(SM)

IVENEER LTD

Dental matrix band, single-use

• Primary Device ID: 7290019259336
• NIH Device Record Key: 4ecc6c82-9756-46d9-a200-cca72dc9c95d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeneerNow Injectable Matrix System
• Version Model Number: Premier Refill 12 SM
• Catalog Number: 9069336
• Company DUNS: 600811880
• Company Name: IVENEER LTD
• Device Count: 6
• DM Exempt: false
• Pre-market Exempt: true
• 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: 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: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com
• Phone: +972524466628
• Email: damir@iveneer.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290019259336 [Primary]
GS1	7290019259336 [Unit of Use]

FDA Product Code

• JEP: Retainer, Matrix

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: 2024-10-29
• Device Publish Date: 2024-10-21

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• 7290019259374: 6(ML)
• 7290019259367: 6(ML)
• 7290019259350: 6(ML)
• 7290019259343: 6(ML)
• 7290019259336: 6(SM)
• 7290019259329: 6(SM)
• 7290019259312: 6(SM)
• 7290019259305: 6(SM)
• 7290019259299: 6(SM)
• 7290019259282: 6(SM)
• 7290019259275: 6(SM)
• 7290019259268: 6(SM)
• 7290019259251: 2 (SM)