ILED 3K / TRUVIDIA/VIDIAPORT 4028210

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-28 for ILED 3K / TRUVIDIA/VIDIAPORT 4028210 manufactured by Trumpf Medizin Systeme Gmbh + Co. Kg.

Event Text Entries

[112851789] It is known that improper installation, maintenance or a collision can lead to the spring arm joint cover falling. The device is still being investigated by an olympus (b)(4) technician. A follow-up report will be submitted if new pertinent information is obtained.
Patient Sequence No: 1, Text Type: N, H10


[112851790] During an unspecified procedure, the plastic strip of a iled 3k's ac3000 arm joint cover fell near the sterile field. No patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9681407-2018-00031
MDR Report Key7645307
Date Received2018-06-28
Date of Report2018-05-29
Date of Event2018-05-29
Date Mfgr Received2018-05-29
Device Manufacturer Date2009-07-22
Date Added to Maude2018-06-28
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. STEFFEN ULBRICH
Manufacturer StreetCARL-ZEISS STRASSE 7-9
Manufacturer CitySAALFELD, 07318
Manufacturer CountryGM
Manufacturer Postal07318
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameILED 3K / TRUVIDIA/VIDIAPORT
Generic NameILED 3K
Product CodeFQP
Date Received2018-06-28
Model Number4028210
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTRUMPF MEDIZIN SYSTEME GMBH + CO. KG
Manufacturer AddressCARL-ZEISS STRASSE 7-9 SAALFELD, 07318 GM 07318


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-28

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