Flex Cup and Flex Disc

GUDID 00851906007255

Flex Discovery Kit Full Fit, 1 Full Fit Flex Cup and 2 Flex Discs (English only)

FLEX COMPANY, THE

Menstrual cup, non-latex, single-use
Primary Device ID00851906007255
NIH Device Record Key546c79bc-5626-4de1-ae4e-68e97ea5320b
Commercial Distribution StatusIn Commercial Distribution
Brand NameFlex Cup and Flex Disc
Version Model NumberFlex Discovery Kit Full Fit
Company DUNS080314616
Company NameFLEX COMPANY, THE
Device Count3
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com
Phone18009310882
Emailhello@flexfits.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100851906007040 [Unit of Use]
GS100851906007255 [Primary]
GS110851906007252 [Package]
Package: Inner Pack [3 Units]
In Commercial Distribution
GS120851906007259 [Package]
Contains: 10851906007252
Package: Case [6 Units]
In Commercial Distribution

FDA Product Code

HHECup, Menstrual

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-03-22
Device Publish Date2019-03-14

On-Brand Devices [Flex Cup and Flex Disc]

20851906007266Flex Discovery Kit Slim Fit, 1 Slim Fit Flex Cup and 2 Flex Discs (English only)
00851906007255Flex Discovery Kit Full Fit, 1 Full Fit Flex Cup and 2 Flex Discs (English only)

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.