LUCOOLIFE

GUDID 06970240895503

Ningbo Luke Medical Devices Co., Ltd.

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	06970240895503
NIH Device Record Key	6199bed4-33f5-4335-8fd5-79623768d654
Commercial Distribution Status	In Commercial Distribution
Brand Name	LUCOOLIFE
Version Model Number	Pink-T/S/L
Company DUNS	541284393
Company Name	Ningbo Luke Medical Devices Co., Ltd.
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	06970240895503 [Primary]

FDA Product Code

HHE	Cup, Menstrual