Nella VuLight

GUDID 00860000270441

Single Use LED Illuminator

CEEK WOMEN'S HEALTH

Hand-held examination/treatment light
Primary Device ID00860000270441
NIH Device Record Key03d20b6e-2e72-437b-b659-9a9c5e02c9cf
Commercial Distribution StatusIn Commercial Distribution
Brand NameNella VuLight
Version Model NumberVL050
Company DUNS116951931
Company NameCEEK WOMEN'S HEALTH
Device Count50
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com
Phone3309909065
Emailmlalli@ceekwomenshealth.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100860000270410 [Primary]
GS100860000270441 [Unit of Use]

FDA Product Code

KYTLight, Examination, Medical, Battery Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-04
Device Publish Date2020-08-27