RESOUND PZ861-DRWC 20928601

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 2020-01-13 for RESOUND PZ861-DRWC 20928601 manufactured by Gn Hearing A/s.

Event Text Entries

[178316141] S/n (b)(4), left. Manufacturing date 07/30/2019 for s/n (b)(4), left.
Patient Sequence No: 1, Text Type: N, H10


[178316142] Severe allergic reaction from the semi-open domes, scaling of the skin. End-user has seen a doctor twice. Antibiotics have been prescribed. Both ears were affected.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005650109-2020-00002
MDR Report Key9581421
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-13
Date of Report2020-01-13
Date Mfgr Received2019-12-14
Device Manufacturer Date2019-06-26
Date Added to Maude2020-01-13
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 ContactMR. LARS HAGANDER
Manufacturer StreetLAUTRUPBJERG 7
Manufacturer CityBALLERUP, COPENHAGEN 2750
Manufacturer CountryDA
Manufacturer Postal2750
Manufacturer G1GN HEARING A/S
Manufacturer StreetLAUTRUPBJERG 7
Manufacturer CityBALLERUP, 2750
Manufacturer CountryDA
Manufacturer Postal Code2750
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRESOUND
Generic NamePREZA 8
Product CodeOSM
Date Received2020-01-13
Model NumberPZ861-DRWC
Catalog Number20928601
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerGN HEARING A/S
Manufacturer AddressLAUTRUPBJERG 7 BALLERUP, 2750 DA 2750


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-13

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