Tabletop Waterpik Adapter Wands 27210

GUDID 10859911004792

Tabletop Waterpik Adapter Wands

Bionix, LLC

Ear canal irrigation kit, reusable
Primary Device ID10859911004792
NIH Device Record Keyc855d58a-9986-4466-b347-17a2f8ece7d5
Commercial Distribution Discontinuation2025-09-08
Commercial Distribution StatusNot in Commercial Distribution
Brand NameTabletop Waterpik Adapter Wands
Version Model Number27210
Catalog Number27210
Company DUNS117844489
Company NameBionix, LLC
Device Count3
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
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)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com
Phone+1(800)551-7096
EmailBionix@bionix.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100859911004795 [Primary]
GS110859911004792 [Unit of Use]

FDA Product Code

LRDAPPLICATOR, ENT DRUG

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2025-09-09
Device Publish Date2024-07-11

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