PENTAX FI-16RBS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-19 for PENTAX FI-16RBS manufactured by Hoya Corporation Pentax Tokyo Office.

MAUDE Entry Details

Report Number9610877-2019-00224
MDR Report Key8712000
Date Received2019-06-19
Date of Report2019-02-01
Date of Event2019-02-01
Date Facility Aware2019-02-01
Report Date2019-06-19
Date Reported to FDA2019-06-19
Date Reported to Mfgr2019-06-19
Date Mfgr Received2019-02-01
Device Manufacturer Date2004-03-22
Date Added to Maude2019-06-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. WILLIAM GOELLER (TEMPORARY)
Manufacturer Street3 PARAGON DRIVE
Manufacturer CityMONTVALE NJ 07645
Manufacturer CountryUS
Manufacturer Postal07645
Manufacturer Phone8004315880
Manufacturer G1HOYA CORPORATION PENTAX TOKYO OFFICE
Manufacturer StreetTSUTSUJIGAOKA 1-1-110 AKISHIMA-SHI
Manufacturer CityTOKYO, 196-0012
Manufacturer CountryJA
Manufacturer Postal Code196-0012
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePENTAX
Generic NameFIBER INTUBATION SCOPE
Product CodeCAL
Date Received2019-06-19
Model NumberFI-16RBS
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age15 YR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHOYA CORPORATION PENTAX TOKYO OFFICE
Manufacturer AddressTSUTSUJIGAOKA 1-1-110 AKISHIMA-SHI TOKYO, 196-0012 JA 196-0012


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-19

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