BENCO ADMIX 5122303

GUDID 29336472004860

BENCO ADMIX 2SP REG 500

SDI LIMITED

Dental amalgam alloy

• Primary Device ID: 29336472004860
• NIH Device Record Key: c8465123-50e7-416a-b90f-8ec227c1357b
• Commercial Distribution Discontinuation: 2026-02-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: BENCO ADMIX
• Version Model Number: 5122303
• Catalog Number: 5122303
• Company DUNS: 753221852
• Company Name: SDI LIMITED
• 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: true
• 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	29336472004860 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032152

FDA Product Code

• EJJ: Alloy, Amalgam

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: 2026-02-25
• Device Publish Date: 2026-02-17

On-Brand Devices [BENCO ADMIX]

• 29336472004860: BENCO ADMIX 2SP REG 500
• 29336472004747: BENCO ADMIX 2SP REG 50