Primary Device ID | D003907991 |
NIH Device Record Key | 47228e4d-1818-4bef-ab80-28ab2c016ed3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Nupro Freedom™ |
Version Model Number | 90799 |
Catalog Number | 90799 |
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 Issuing Agency | Device ID |
---|---|
HIBCC | D003907991 [Primary] |
EKX | Handpiece, direct drive, ac-powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-05 |
Device Publish Date | 2022-11-25 |
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 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NUPRO FREEDOM 85510725 4154235 Live/Registered |
DENTSPLY SIRONA INC. 2012-01-06 |
NUPRO FREEDOM 85294315 4081391 Live/Registered |
DENTSPLY SIRONA INC. 2011-04-13 |