Equate

GUDID 00681131156066

Personal Lubricant

GUY & O'NEILL, INC.

Sexual lubricant
Primary Device ID00681131156066
NIH Device Record Key7fd4a0d6-3649-4b67-9804-66a658865167
Commercial Distribution StatusIn Commercial Distribution
Brand NameEquate
Version Model Number900-050
Company DUNS037838844
Company NameGUY & O'NEILL, INC.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com
Phone479-204-8686
EmailTiffany.Burnett@walmart.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100681131156066 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUCLubricant, Personal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-08-09
Device Publish Date2017-04-19