BAUSH & LOMB

GUDID 04719872850175

BONASSE ENTERPRISES CO., LTD.

Contact lens case
Primary Device ID04719872850175
NIH Device Record Keyaf03d819-cd1a-4269-872a-64142ec6cf99
Commercial Distribution StatusIn Commercial Distribution
Brand NameBAUSH & LOMB
Version Model NumberSC-160
Company DUNS657544912
Company NameBONASSE ENTERPRISES CO., LTD.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Safe
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
GS104719872850175 [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 Date2016-09-14

Devices Manufactured by BONASSE ENTERPRISES CO., LTD.

04719872850014 - BONASSE 2018-07-06
04719872850038 - BONASSE2018-07-06
04719872850052 - BONASSE 2018-07-06
04719872850069 - BONASSE2018-07-06
04719872850076 - Voguestrap 2018-07-06
04719872850113 - Voguestrap 2018-07-06
04719872850137 - VOGUESTRAP2018-07-06
04719872850168 - BONASSE 2018-07-06

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