CERABALT K40

GUDID 03760357970186

BERNARD CERVOS SOCIETE

Dental casting non-noble alloy

• Primary Device ID: 03760357970186
• NIH Device Record Key: f04e64d0-b4b3-426f-bd21-99ca28eb2ed6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CERABALT K40
• Version Model Number: Ingots 15x8 mm
• Company DUNS: 346973803
• Company Name: BERNARD CERVOS SOCIETE
• Device Count: 1
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760357970186 [Primary]

FDA Product Code

• EJH: Alloy, Metal, Base

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: 2024-07-01
• Device Publish Date: 2024-06-21

Devices Manufactured by BERNARD CERVOS SOCIETE

• 03760357972630 - NICRALLIUM N7: 2024-07-08
• 03760357975075 - NICRALLIUM N4: 2024-07-08
• 03760357975082 - NICRALLIUM N4: 2024-07-08
• 03760357975099 - NICRALLIUM N4: 2024-07-08
• 03760357970025 - CERABALT K30: 2024-07-01
• 03760357970049 - NICRALLIUM N2: 2024-07-01
• 03760357970063 - CERINOX C10: 2024-07-01
• 03760357970186 - CERABALT K40: 2024-07-01
• 03760357970186 - CERABALT K40: 2024-07-01