Nella VuLight

GUDID 10860000270448

Single Use LED Illuminator

CEEK WOMEN'S HEALTH

Hand-held examination/treatment light
Primary Device ID10860000270448
NIH Device Record Key0c6a8d66-ba95-4fd0-b6cb-3a1e47f2f4c2
Commercial Distribution StatusIn Commercial Distribution
Brand NameNella VuLight
Version Model NumberVL005
Company DUNS116951931
Company NameCEEK WOMEN'S HEALTH
Device Count5
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
GS100860000270441 [Unit of Use]
GS110860000270448 [Primary]

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