Beta Mini

GUDID 08800019101659

B& L Biotech, inc.

Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system Endodontic obturation system

• Primary Device ID: 08800019101659
• NIH Device Record Key: 3815e8a4-72b4-4a1d-b8cb-cd492255f478
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Beta Mini
• Version Model Number: BP-B1
• Company DUNS: 687338285
• Company Name: B& L Biotech, inc.
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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	08800019101659 [Primary]

FDA Product Code

• EKR: Plugger, Root Canal, Endodontic

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: 2020-06-23
• Device Publish Date: 2020-06-15

On-Brand Devices [Beta Mini]

• 08800019101154: BP-B1
• 08800019101659: BP-B1