nixit

GUDID 00627987071368

Nixit Limited

Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable Menstrual cup, non-latex, reusable

Primary Device ID	00627987071368
NIH Device Record Key	7cd830b3-a311-4ef8-a56d-9cb74027e9a5
Commercial Distribution Status	In Commercial Distribution
Brand Name	nixit
Version Model Number	00627987071368
Company DUNS	204591013
Company Name	Nixit Limited
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00627987071368 [Primary]

FDA Product Code

HHE	Cup, Menstrual