Johnson-Promident

GUDID 00862314000394

ultrasonic scaling insert

JOHNSON-PROMIDENT

Ultrasonic dental scaling/debridement system handpiece tip, periodontal

• Primary Device ID: 00862314000394
• NIH Device Record Key: b445eea0-df89-4605-aa9e-745047522d34
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Johnson-Promident
• Version Model Number: UI-FS10030
• Company DUNS: 965230188
• Company Name: JOHNSON-PROMIDENT
• 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: 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00862314000394 [Primary]

FDA Product Code

• ELC: Scaler, Ultrasonic

Sterilization

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

[00862314000394]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-06

On-Brand Devices [Johnson-Promident]

• 00862314000394: ultrasonic scaling insert
• 00862314000387: ultrasonic scaling insert
• 00862314000370: ultrasonic scaling insert
• 00862314000363: ultrasonic scaling insert
• 00862314000356: ultrasonic scaling insert
• 00862314000349: ultrasonic scaling insert
• 00862314000332: ultrasonic scaling insert
• 00862314000325: ultrasonic scaling insert
• 00862314000318: ultrasonic scaling insert