EOS CobaltChrome SP2

GUDID 06430038380180

EOS CobaltChrome SP2 is cobalt based metal-ceramic alloy intended for production of Porcelain-Fused to Metal (PFM) dental restorations (crowns, bridge

Electro Optical Systems Finland Oy

Dental casting non-noble alloy

• Primary Device ID: 06430038380180
• NIH Device Record Key: b6e233f1-08c8-43e2-a359-05d5bcf3ec57
• Commercial Distribution Discontinuation: 2020-06-01
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EOS CobaltChrome SP2
• Version Model Number: 9011-0018
• Company DUNS: 369507723
• Company Name: Electro Optical Systems Finland Oy
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06430038380180 [Primary]

FDA Product Code

• EJH: Alloy, Metal, Base

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-11
• Device Publish Date: 2016-09-24

On-Brand Devices [EOS CobaltChrome SP2]

• 06430038380470: EOS CobaltChrome SP2 is cobalt based metal-ceramic alloy intended for production of Porcelain-Fu
• 06430038380180: EOS CobaltChrome SP2 is cobalt based metal-ceramic alloy intended for production of Porcelain-Fu