HF-RESECTION ELECTRODE "PLASMALOOP", LOOP, MEDIUM, 24 FR., 12?/16?, ESG TURIS WA22702S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other,use report with the FDA on 2020-03-26 for HF-RESECTION ELECTRODE "PLASMALOOP", LOOP, MEDIUM, 24 FR., 12?/16?, ESG TURIS WA22702S manufactured by Olympus Winter & Ibe Gmbh.

MAUDE Entry Details

Report Number9610773-2020-00098
MDR Report Key9884983
Report SourceHEALTH PROFESSIONAL,OTHER,USE
Date Received2020-03-26
Date of Report2020-03-26
Date Mfgr Received2020-03-03
Device Manufacturer Date2019-05-30
Date Added to Maude2020-03-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. DANIEL WLADOW
Manufacturer StreetKUEHNSTRASSE 61
Manufacturer CityHAMBURG 22045
Manufacturer CountryGM
Manufacturer Postal22045
Manufacturer Phone4940669662
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHF-RESECTION ELECTRODE "PLASMALOOP", LOOP, MEDIUM, 24 FR., 12?/16?, ESG TURIS
Generic NameRESECTION ELECTRODES WITH HF CABLE
Product CodeFAS
Date Received2020-03-26
Model NumberWA22702S
Lot Number1000042426
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS WINTER & IBE GMBH
Manufacturer AddressKUEHNSTRASSE 61 HAMBURG, HAMBURG 22045 GM 22045


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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