FDA Adverse Event No answer provided Summary report: N

HAMILTON

MDR report key: 11211047 · Received January 21, 2021

Report

Report Number
0002937708-2021-00004
Event Type
No answer provided
Date Received
January 21, 2021
Date of Event
December 12, 2020
Report Date
August 15, 2022
Manufacturer
HAMILTON MEDICAL AG
Product Code
CBK
UDI-DI
07630002800761
Report Source
Distributor report
Reporter Location
NV, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

INCLUDED UDI IN REPORT.

Description of Event or Problem · 0

TF 246005 DURING VENTILATION.

Description of Event or Problem · 1

TF 246005 DURING VENTILATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
102746 HAMILTON HAMILTON-MR1 CBK HAMILTON MEDICAL AG 161010 07630002800761

Patients

Seq Age Sex Outcome Treatment
1 Unknown