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.
Report Number | 9681154-2020-00003 |
MDR Report Key | 9746315 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-02-24 |
Date of Report | 2020-02-21 |
Date Mfgr Received | 2020-02-21 |
Device Manufacturer Date | 2016-12-05 |
Date Added to Maude | 2020-02-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR ADAM PRICE |
Manufacturer Street | CHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE |
Manufacturer City | CHICHESTER, PO202FT |
Manufacturer Country | UK |
Manufacturer Postal | PO20 2FT |
Manufacturer G1 | RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD |
Manufacturer Street | CHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE |
Manufacturer City | CHICHESTER, PO202FT |
Manufacturer Country | UK |
Manufacturer Postal Code | PO20 2FT |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INNOSPIRE ESSENCE |
Generic Name | NEBULIZER |
Product Code | CAF |
Date Received | 2020-02-24 |
Returned To Mfg | 2020-02-13 |
Model Number | 1100312 |
Catalog Number | 1100312 |
Lot Number | 161205 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | RESPIRONICS RESPIRATORY DRUG DELIVERY (UK) LTD |
Manufacturer Address | CHICHESTER BUSINESS PARK CITY FIELDS WAY, TANGMERE CHICHESTER, PO202FT UK PO20 2FT |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-24 |