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Device Recall OERPro Endoscope Reprocessor
Model / Serial
Model: OER-Pro, All serial numbers affected
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Distributed to: AK,AL,AR,AZ,CA,CO,CT,DC,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,RI,SC,TN,TX,UT,VA,VT,WA,WI,WV,WY
Product Description
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Manufacturer
Olympus Corporation of the Americas
1 Event
Recall of Device Recall OERPro Endoscope Reprocessor
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Manufacturer
Olympus Corporation of the Americas
Manufacturer Address
Olympus Corporation of the Americas, 3500 Corporate Pkwy, PO Box 610, Center Valley PA 18034-0610
Manufacturer Parent Company (2017)
Olympus Corporation
Source
USFDA
Language
English
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