750-600 05342716001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-12-22 for 750-600 05342716001 manufactured by Ventana Medical Systems Inc.

Event Text Entries

[63497659] Similar case reported under mfr report ref # (b)(4) on 6/2/2016.
Patient Sequence No: 1, Text Type: N, H10


[63497660] Instrument malfunction "leak" without adverse event. No reports of slip/fall or injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2028492-2016-00006
MDR Report Key6199730
Date Received2016-12-22
Date of Report2016-12-22
Date of Event2016-11-30
Date Mfgr Received2016-11-30
Date Added to Maude2016-12-22
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 ContactNA TIM GIBLIN
Manufacturer Street1910 E INNOVATION PARK DRIVE NA
Manufacturer CityTUSCON AZ 85755
Manufacturer CountryUS
Manufacturer Postal85755
Manufacturer Phone5208777035
Manufacturer G1VENTANA MEDICAL SYSTEMS INC
Manufacturer Street1910 E INNOVATION PARK DR NONE
Manufacturer CityTUCSON AZ 857551962
Manufacturer CountryUS
Manufacturer Postal Code857551962
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report0

Device Details

Generic NameBENCHMARK ULTRA
Product CodeKPA
Date Received2016-12-22
Model Number750-600
Catalog Number05342716001
Lot NumberNA
ID NumberUDI 04015630981052
OperatorOTHER HEALTH CARE PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerVENTANA MEDICAL SYSTEMS INC
Manufacturer Address1910 E INNOVATION PARK DR NA TUCSON AZ 857551962 US 857551962


Patients

Patient NumberTreatmentOutcomeDate
10 2016-12-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.