CUTTER HARDENER UNIVERSAL PLUS PASTE 66037444

GUDID J014660374440

Material impression

Heraeus Kulzer GmbH

Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material Polyether dental impression material

• Primary Device ID: J014660374440
• NIH Device Record Key: 02838dcb-b3f7-446b-aaed-43017be7d85c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CUTTER HARDENER UNIVERSAL PLUS PASTE
• Version Model Number: 66037444
• Catalog Number: 66037444
• Company DUNS: 315666321
• Company Name: Heraeus Kulzer GmbH
• Device Count: 1
• DM Exempt: true
• 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: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx
• Phone: +1(800)431-1785
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	J014660374440 [Primary]

FDA Product Code

• ELW: MATERIAL, IMPRESSION

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-10-30
• Device Publish Date: 2016-09-15

Devices Manufactured by Heraeus Kulzer GmbH

• J014660354840 - Venus Diamond: 2024-03-14 VENUS DIAMOND SYRINGE REFILL 1x4G OL
• J014660354850 - Venus Diamond: 2024-03-14 VENUS DIAMOND SYRINGE REFILL 1x4G OM
• J014660354860 - Venus Diamond: 2024-03-14 VENUS DIAMOND SYRINGE REFILL 1x4G OD
• J014660390210 - Venus Diamond: 2024-03-14 VENUS DIAMOND PLT REFILL 1x10x0,25G OL
• J014660390220 - Venus Diamond: 2024-03-14 VENUS DIAMOND PLT REFILL 2x10x0,25G OM
• J014660390230 - Venus Diamond: 2024-03-14 VENUS DIAMOND PLT REFILL 2x10x0,25G OD
• J014660982750 - Venus Diamond: 2024-03-14 PROC Venus Diamond Kit 2x20X0.25G PLT
• J014660982760 - Venus Pearl: 2024-03-14 PROC Venus Pearl Kit 2x20X0.2G PLT