FOOT RELEASE

GUDID 04953170022975

OLYMPUS MEDICAL SYSTEMS CORP.

Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical Foot-switch, electrical
Primary Device ID04953170022975
NIH Device Record Key86b83a1c-ea6c-4c4c-90f8-8ff495ab9a4a
Commercial Distribution StatusIn Commercial Distribution
Brand NameFOOT RELEASE
Version Model NumberMB-332
Company DUNS711789789
Company NameOLYMPUS MEDICAL SYSTEMS CORP.
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx
Phone+1(800)401-1086
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS104953170022975 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FDTduodenoscope and accessories, flexible/rigid

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 Date2016-09-21

Devices Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

04953170452932 - TRACHEAL INTUBATION FIBERSCOPE2024-04-22
14953170460064 - Single Use Biliary Drainage Stent V2024-04-02
14953170460088 - Single Use Biliary Drainage Stent V2024-04-02
14953170460101 - Single Use Biliary Drainage Stent V2024-04-02
14953170460132 - Single Use Biliary Drainage Stent V2024-04-02
14953170460330 - Single Use Biliary Drainage Stent V2024-04-02
14953170460378 - Single Use Biliary Drainage Stent V2024-04-02
14953170460613 - Single Use Biliary Drainage Stent V2024-04-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.