Cavex Orthotrace AA380

GUDID E241AA3800

Dental Alginate Impression material

Cavex Holland B.V.

Alginate dental impression material

• Primary Device ID: E241AA3800
• NIH Device Record Key: 40a1f4b9-240c-4e86-9056-e5a8b05ff97d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cavex Orthotrace
• Version Model Number: AA380
• Catalog Number: AA380
• Company DUNS: 419980156
• Company Name: Cavex Holland B.V.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: +31(0)235307700
• Email: r.woortman@cavex.nl

Device Dimensions

• Weight: 500 Gram

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	E241AA3800 [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: 2016-06-09

On-Brand Devices [Cavex Orthotrace]

• E241AA3831: Dental Alginate Impression material
• E241AA3830: Dental Alginate Impression material
• E241AA3801: Dental Alginate Impression material
• E241AA3800: Dental Alginate Impression material