ADHERUS AUTOSPRAY NUS-106

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-10 for ADHERUS AUTOSPRAY NUS-106 manufactured by Hyperbranch Medical Technology, Inc.

MAUDE Entry Details

Report Number0008010177-2019-00033
MDR Report Key8684750
Date Received2019-06-10
Date of Report2019-06-10
Date of Event2019-05-14
Date Mfgr Received2019-05-14
Date Added to Maude2019-06-10
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. RYLEE KOOLE
Manufacturer StreetBOETZINGERSTR. 41
Manufacturer CityFREIBURG D-79111
Manufacturer PostalD-79111
Manufacturer Phone76145120
Manufacturer G1HYPERBRANCH MEDICAL TECHNOLOGY, INC
Manufacturer Street800-12 CAPITOLA DRIVE
Manufacturer CityDURHAM NC 27713
Manufacturer CountryUS
Manufacturer Postal Code27713
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameADHERUS AUTOSPRAY
Generic NameIMPLANT
Product CodeNQR
Date Received2019-06-10
Catalog NumberNUS-106
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerHYPERBRANCH MEDICAL TECHNOLOGY, INC
Manufacturer Address800-12 CAPITOLA DRIVE DURHAM NC 27713 US 27713


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-06-10

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