COLLECT.NO.QAS HIP STEMS CENTEGA/ANTEGA AE-QAS-H546-26

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-18 for COLLECT.NO.QAS HIP STEMS CENTEGA/ANTEGA AE-QAS-H546-26 manufactured by Aesculap Ag.

Event Text Entries

[111847393] (b)(4). Manufacturing site evaluation: evaluation on-going. Device not returned
Patient Sequence No: 1, Text Type: N, H10


[111847394] (b)(6). It was reported that 23y po fractured antega shaft.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610612-2018-00261
MDR Report Key7611563
Date Received2018-06-18
Date of Report2018-06-18
Date of Event2018-05-15
Date Facility Aware2018-06-11
Date Mfgr Received2018-05-22
Date Added to Maude2018-06-18
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 ContactMS. NICOLE BROYLES
Manufacturer Street615 LAMBERT POINTE DRIVE
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer G1AESCULAP AG
Manufacturer StreetPO BOX 40
Manufacturer CityTUTTLINGEN, 78501
Manufacturer CountryGM
Manufacturer Postal Code78501
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCOLLECT.NO.QAS HIP STEMS CENTEGA/ANTEGA
Generic NameMPLANTS ANTEGA / CENTEGA
Product CodeELE
Date Received2018-06-18
Model NumberAE-QAS-H546-26
Catalog NumberAE-QAS-H546-26
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAESCULAP AG
Manufacturer AddressPO BOX 40 TUTTLINGEN, 78501 GM 78501


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-06-18

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