BAIR HUGGER 36000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-31 for BAIR HUGGER 36000 manufactured by 3m Company.

MAUDE Entry Details

Report Number9260088
MDR Report Key9260088
Date Received2019-10-31
Date of Report2019-09-12
Date of Event2019-04-22
Report Date2019-09-12
Date Reported to FDA2019-09-12
Date Reported to Mfgr2019-10-31
Date Added to Maude2019-10-31
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBAIR HUGGER
Generic NameTHERMOMETER, ELECTRONIC, CLINICAL
Product CodeFLL
Date Received2019-10-31
Catalog Number36000
Lot Number19038
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
Manufacturer3M COMPANY
Manufacturer Address3M CENTER, 2510 CONWAY AVE. BLDG. 275-5W-06 SAINT PAUL MN 55144 US 55144


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-31

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