BELLATEK? ENCODE? HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H) EHA444

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-27 for BELLATEK? ENCODE? HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H) EHA444 manufactured by Biomet 3i.

Event Text Entries

[185547473] Zimmer biomet (b)(4) patient weight: not provided. Event date: not provided. Initial reporter fax number: not provided. Device remains in patient's mouth.
Patient Sequence No: 1, Text Type: N, H10


[185547514] It was reported that a healing abutment (eha444) could not seat into the implant. Doctor tried to force the healing abutment down. Healing abutment was left in the patient mouth. Tooth location 14.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001038806-2020-00586
MDR Report Key9890302
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-27
Date of Report2020-03-27
Date Mfgr Received2020-03-03
Device Manufacturer Date2016-09-14
Date Added to Maude2020-03-27
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS SUSANNE TAYLOR
Manufacturer Street4555 RIVERSIDE DRIVE
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal33410
Manufacturer Phone5617766700
Manufacturer G1BIOMET 3I
Manufacturer Street4555 RIVERSIDE DRIVE
Manufacturer CityPALM BEACH GARDENS FL 33410
Manufacturer CountryUS
Manufacturer Postal Code33410
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBELLATEK? ENCODE? HEALING ABUTMENT 4.1MM(D) X 4.1MM(P) X 4MM(H)
Generic NameHEALING ABUTMENT
Product CodeNHA
Date Received2020-03-27
Catalog NumberEHA444
Lot Number1200101
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMET 3I
Manufacturer Address4555 RIVERSIDE DRIVE PALM BEACH GARDENS FL 33410 US 33410


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-27

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