INNOSPIRE ESSENCE 1100312

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 2020-02-24 for INNOSPIRE ESSENCE 1100312 manufactured by Respironics Respiratory Drug Delivery (uk) Ltd.

MAUDE Entry Details

Report Number9681154-2020-00003
MDR Report Key9746315
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-24
Date of Report2020-02-21
Date Mfgr Received2020-02-21
Device Manufacturer Date2016-12-05
Date Added to Maude2020-02-24
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 ADAM PRICE
Manufacturer StreetCHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE
Manufacturer CityCHICHESTER, PO202FT
Manufacturer CountryUK
Manufacturer PostalPO20 2FT
Manufacturer G1RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD
Manufacturer StreetCHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE
Manufacturer CityCHICHESTER, PO202FT
Manufacturer CountryUK
Manufacturer Postal CodePO20 2FT
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINNOSPIRE ESSENCE
Generic NameNEBULIZER
Product CodeCAF
Date Received2020-02-24
Returned To Mfg2020-02-13
Model Number1100312
Catalog Number1100312
Lot Number161205
OperatorLAY USER/PATIENT
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerRESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD
Manufacturer AddressCHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE CHICHESTER, PO202FT UK PO20 2FT


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-24

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