EVIS EXERA III BRONCHOFIBERVIDEOSCOPE

GUDID 04953170395581

OLYMPUS MEDICAL SYSTEMS CORP.

Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope Flexible fibreoptic bronchoscope
Primary Device ID04953170395581
NIH Device Record Keyf9ab9934-d4fd-4348-85a5-1bf28457deeb
Commercial Distribution StatusIn Commercial Distribution
Brand NameEVIS EXERA III BRONCHOFIBERVIDEOSCOPE
Version Model NumberOLYMPUS BF-MP190F
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 Batchfalse
Serial Numbertrue
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
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
GS104953170395581 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EOQBronchoscope (flexible or rigid)

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


[04953170395581]

Ethylene Oxide;High-level Disinfectant


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-07-12
Device Publish Date2018-06-11

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