BONASIL A+ Heavy

GUDID 05206569530049

Addition curing vinyl polysiloxane impression material

DMP DENTAL INDUSTRY S.A.

Silicone dental impression material

• Primary Device ID: 05206569530049
• NIH Device Record Key: c97ca910-d14b-404a-b08d-612e321cc820
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BONASIL A+ Heavy
• Version Model Number: 380ml
• Company DUNS: 728534814
• Company Name: DMP DENTAL INDUSTRY S.A.
• 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: 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: +302299023041
• Email: info@dmpdental.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 10 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	05206569530025 [Primary]
GS1	05206569530049 [Package]; Contains: 05206569530025; Package: Box [2 Units]; In Commercial Distribution

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: 2016-09-24

On-Brand Devices [BONASIL A+ Heavy]

• 05206569530049: Addition curing vinyl polysiloxane impression material
• 05206569530063: Addition curing vinyl polysiloxane impression material
• 05206569530032: Addition curing vinyl polysiloxane impression material