orthoprint C302145

GUDID EZHIC3021450

Alginate impression material

ZHERMACK SPA

Alginate dental impression material

• Primary Device ID: EZHIC3021450
• NIH Device Record Key: cdbb477e-f4e4-4cf3-a3cb-24a61baeb0e9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: orthoprint
• Version Model Number: C302145
• Catalog Number: C302145
• Company DUNS: 432971034
• Company Name: ZHERMACK SPA
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: +390425597611
• Email: info@zhermack.com

Device Dimensions

• Device Size Text, specify: 0

Operating and Storage Conditions

• Storage Environment Temperature: Between 5 Degrees Celsius and 27 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	EZHIC3021450 [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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-09

On-Brand Devices [orthoprint]

• EZHISP500531: Alginate impression material
• EZHIC3021710: Alginate impression material
• EZHIC3021611: Alginate impression material
• EZHIC3021601: Alginate impression material
• EZHIC3021450: Alginate impression material