YASARGIL TI PERM STD-CLIP BAYO 12MM FT759T

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2014-10-02 for YASARGIL TI PERM STD-CLIP BAYO 12MM FT759T manufactured by Aesculap Ag & Co. Kg.

Event Text Entries

[21238942] Country of complaint: (b)(6). Complaint states: when the surgeon clipped the bump, scissoring was occurred.
Patient Sequence No: 1, Text Type: D, B5


[21372953] Mfg site eval: eval is ongoing.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2916714-2014-00736
MDR Report Key4284208
Report Source01,07
Date Received2014-10-02
Date of Report2014-10-01
Date of Event2014-06-04
Date Mfgr Received2014-06-05
Device Manufacturer Date2013-01-21
Date Added to Maude2014-12-02
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMICHELLE LINK
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3145515938
Manufacturer G1AESCULAP AG&CO KG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use0
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameYASARGIL TI PERM STD-CLIP BAYO 12MM
Product CodeHCH
Date Received2014-10-02
Model NumberFT759T
Catalog NumberFT759T
Lot Number4505410194
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG & CO. KG
Manufacturer AddressTUTTLINGEN 78532 GM 78532


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2014-10-02

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