Nupro Freedom™ 90742

GUDID D003907421

Nupro Freedom™ Wireless Foot Pedal, Spare

Dentsply Professional

Ultrasonic dental scaling/debridement system handpiece

• Primary Device ID: D003907421
• NIH Device Record Key: 9eec0c80-9165-43cc-958d-29ad426f7e37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nupro Freedom™
• Version Model Number: 90742
• Catalog Number: 90742
• Company DUNS: 144140845
• Company Name: Dentsply Professional
• 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: true
• 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
HIBCC	D003907421 [Primary]

FDA Product Code

• EKX: Handpiece, direct drive, ac-powered

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: 2022-12-05
• Device Publish Date: 2022-11-25

On-Brand Devices [Nupro Freedom™]

• D003907991: Nupro Freedom™ Inner Module, Lavender, Spare
• D003907981: Nupro Freedom™ Power Adapter
• D003907971: Nupro Freedom™ Charging Base, Lavender Spares
• D003907961: Nupro Freedom™ Outer Sheath, Spare
• D003907421: Nupro Freedom™ Wireless Foot Pedal, Spare