Biotec

GUDID 00860011235002

Dental Control Unit

Biotec Incorporated

Dental delivery system instrument unit, pneumatic

• Primary Device ID: 00860011235002
• NIH Device Record Key: d1f87ce5-8fc1-444a-9937-91cae63b8342
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Biotec
• Version Model Number: Control Unit
• Company DUNS: 047148853
• Company Name: Biotec Incorporated
• 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: 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	00860011235002 [Primary]

FDA Product Code

• EIA: Unit, Operative Dental

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: 2024-01-26
• Device Publish Date: 2024-01-18