DEVICE: Pro-Select Platinum® (D813S30500)
Device Identifier (DI) Information
Pro-Select Platinum®
S30500
In Commercial Distribution
S30500
DEN-MAT HOLDINGS, LLC
S30500
In Commercial Distribution
S30500
DEN-MAT HOLDINGS, LLC
Transformer/Adapter + Wall Plug (Universal for PSP & PS3)
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
No | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
36047 | Ultrasonic dental scaling/debridement system |
An assembly of mains electricity (AC-powered) devices intended to apply ultrasonic oscillations to: 1) mechanically fragment and dislodge gross debris in the dental pulp canal during an endodontic procedure; and/or 2) remove accretions from tooth surfaces during dental cleaning/periodontal therapy. The system typically consists of a generator with controls (e.g., foot-switch) that produces and controls high frequency electric current, and may provide fluid irrigation; a handpiece used to convert the energy to ultrasonic oscillations; and a tip(s) intended to apply the oscillations to the procedure site; tip selection typically affects the intended application (endodontic vs periodontal).
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
ELC | Scaler, Ultrasonic |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
K964596 | 000 |
Sterilization
No
Yes
CLOSE
Yes
Sterilization Method [?] |
---|
Liquid Chemical |
Moist Heat or Steam Sterilization |
High-level Disinfectant |
Storage and Handling
[?]Storage and Handling |
---|
Special Storage Condition, Specify: Keep Dry |
Special Storage Condition, Specify: Keep away from explosive substances and flammable materials |
Special Storage Condition, Specify: Do not use this product in presence of inflammable anesthetics or gases |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
63fa6faa-c480-4846-b253-ba98469d8ef0
July 06, 2018
3
September 24, 2016
July 06, 2018
3
September 24, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
1-800-433-6628
info@denmat.com
info@denmat.com