PWR Piezo

GUDID 10889950142568

PWR Piezo Unit

HU-FRIEDY MFG. CO., LLC

Ultrasonic dental scaling/debridement system
Primary Device ID10889950142568
NIH Device Record Keyf36d2bbf-3bcd-4b42-bfe5-5de18e0065dc
Commercial Distribution StatusIn Commercial Distribution
Brand NamePWR Piezo
Version Model NumberUPPIEZO
Company DUNS005085972
Company NameHU-FRIEDY MFG. CO., LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com
Phone+1(800)483-7433
Emailinfo@hu-friedy.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110889950142568 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ELCScaler, ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-25
Device Publish Date2024-07-17

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10889950041120 - HU-FRIEDY2025-03-05 RECONDITIONED 23690, DE

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