MIRADRY SYSTEM MD4000-MC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-01-16 for MIRADRY SYSTEM MD4000-MC manufactured by Miradry, Inc..

Event Text Entries

[176608183] Review of lot history records for the involved device confirmed manufacturing steps and processes were met and followed. Product met final inspection and testing requirements prior to shipment. The rate seen (30 worldwide reportable incidents out of estimated 233,000+ procedures performed to date) is approximately 0. 013% of the procedures and within the acceptable range as identified in risk analysis documentations.
Patient Sequence No: 1, Text Type: N, H10


[176608184] Clinic reported a patient who developed hidradenitis suppurativa in right axilla ~5. 8 months post miradry treatment. Symptoms presented at 3 months post-treatment. Antibiotics (keflex 500mg bid) for 10 days and warm compresses on affected area were prescribed. The symptoms resolved.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008082710-2020-00003
MDR Report Key9599353
Report SourceCOMPANY REPRESENTATIVE,CONSUM
Date Received2020-01-16
Date of Report2019-12-18
Date of Event2019-06-26
Date Mfgr Received2019-12-18
Device Manufacturer Date2015-06-02
Date Added to Maude2020-01-16
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 ContactMS. SARA NAKAMURA
Manufacturer Street2790 WALSH AVENUE
Manufacturer CitySANTA CLARA CA 95051
Manufacturer CountryUS
Manufacturer Postal95051
Manufacturer Phone4089408700
Manufacturer G1MIRADRY, INC.
Manufacturer Street2790 WALSH AVENUE
Manufacturer CitySANTA CLARA CA 95051
Manufacturer CountryUS
Manufacturer Postal Code95051
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMIRADRY SYSTEM
Generic NameMICROWAVE DERMATOLOGIC SYSTEM
Product CodeOUB
Date Received2020-01-16
Model NumberMD4000-MC
Catalog NumberMD4000-MC
Lot Number15H0757
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMIRADRY, INC.
Manufacturer Address2790 WALSH AVENUE SANTA CLARA CA 95051 US 95051


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-16

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