#9 DEAN SCISSORS S9

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-11-26 for #9 DEAN SCISSORS S9 manufactured by Hu-friedy Mfg. Co. Llc.

MAUDE Entry Details

Report Number1416605-2019-00018
MDR Report Key9376258
Report SourceHEALTH PROFESSIONAL
Date Received2019-11-26
Date of Report2019-11-26
Date of Event2019-10-31
Date Mfgr Received2019-10-31
Date Added to Maude2019-11-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS STEPHANIE WASIELEWSKI
Manufacturer Street3232 N ROCKWELL ST
Manufacturer CityCHICAGO IL 606185935
Manufacturer CountryUS
Manufacturer Postal606185935
Manufacturer Phone8472574500
Manufacturer G1HU-FRIEDY MFG. CO. LLC
Manufacturer Street3232 N ROCKWELL ST
Manufacturer CityCHICAGO IL 606185935
Manufacturer CountryUS
Manufacturer Postal Code606185935
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name#9 DEAN SCISSORS
Generic NameSCISSORS, SURGICAL TISSUE, DENTAL
Product CodeEGN
Date Received2019-11-26
Model NumberS9
Catalog NumberS9
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHU-FRIEDY MFG. CO. LLC
Manufacturer Address3232 N ROCKWELL ST. CHICAGO IL 606185935 US 606185935


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-11-26

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