ProSilver P-110150

GUDID 07290012207723

Dental Amalgam

SILMET LTD

Dental amalgam

• Primary Device ID: 07290012207723
• NIH Device Record Key: 9cb88a5f-2e33-4792-b022-a5f94ec3eb31
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProSilver
• Version Model Number: P-110150
• Catalog Number: P-110150
• Company DUNS: 600071344
• Company Name: SILMET LTD
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290012207723 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K760980

FDA Product Code

• EJJ: Alloy, Amalgam

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-12-28
• Device Publish Date: 2016-11-09

On-Brand Devices [ProSilver]

• 07290016787658: Dental amalgam powder
• 07290012207730: Dental Amalgam
• 07290012207723: Dental Amalgam
• 07290012207716: Dental Amalgam Alloy
• 07290012207709: Dental Amalgam Alloy
• 07290012207693: Dental Amalgam Alloy