BONASSE

GUDID 04719872850304

BONASSE ENTERPRISES CO., LTD.

Contact lens case
Primary Device ID04719872850304
NIH Device Record Key975e0d81-f5b1-451d-bbb9-51a8c737805b
Commercial Distribution StatusIn Commercial Distribution
Brand NameBONASSE
Version Model NumberBC-790+
Company DUNS657544912
Company NameBONASSE ENTERPRISES CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104719872850304 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LRXCase, Contact Lens

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-12-21

On-Brand Devices [BONASSE]

04719872850311SC-311
04719872850304BC-790+
04719872850298SC-110
04719872850281SC-206
04719872850250G-90
04719872850243LT-192
04719872850236LC-819
04719872850168SC-128
04719872850069SC-212
04719872850052SC-209
04719872850038SC-207
04719872850014SC-201

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