MINIBLASTER

GUDID 00366975000880

MINIBLASTER UNIT

BENCO DENTAL SUPPLY CO.

Dental abrasive air jet system

• Primary Device ID: 00366975000880
• NIH Device Record Key: 9b95ccbe-3913-4ebb-96f2-6b959fed04da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MINIBLASTER
• Version Model Number: 4696-322
• Company DUNS: 015108087
• Company Name: BENCO DENTAL SUPPLY CO.
• 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: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Weight: 215 Gram

Device Identifiers

Device Issuing Agency	Device ID
GS1	00366975000880 [Primary]

FDA Product Code

• KOJ: Airbrush

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-23

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