INNOSPIRE ESSENCE 1100312

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-10-08 for INNOSPIRE ESSENCE 1100312 manufactured by Respironics Respiratory Drug Delivery (uk) Ltd.

MAUDE Entry Details

Report Number9681154-2019-00017
MDR Report Key9166683
Report SourceCONSUMER
Date Received2019-10-08
Date of Report2019-09-16
Date of Event2019-09-16
Date Mfgr Received2019-09-16
Device Manufacturer Date2019-04-12
Date Added to Maude2019-10-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactADAM 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 NameCOMPRESSOR, AIR, PORTABLE
Product CodeBTI
Date Received2019-10-08
Model Number1100312
Catalog Number1100312
Lot Number190412
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
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 2019-10-08

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