USA ELITE CFR TIMBERLAKE OBTURATOR ETO-CFR25

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1999-10-20 for USA ELITE CFR TIMBERLAKE OBTURATOR ETO-CFR25 manufactured by Circon Acmi.

Event Text Entries

[160650] Customer requested warranty review and repair of instrument. Reported that obturator would not completely open every time.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1519132-1999-00076
MDR Report Key246520
Report Source06
Date Received1999-10-20
Date of Report1999-10-20
Date Mfgr Received1999-10-01
Device Manufacturer Date1996-03-01
Date Added to Maude1999-10-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactRONALD EHMSEN, SC.D.
Manufacturer Street6500 HOLLISTER AVENUE
Manufacturer CitySANTA BARBARA CA 93117
Manufacturer CountryUS
Manufacturer Postal93117
Manufacturer Phone*
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameUSA ELITE CFR TIMBERLAKE OBTURATOR
Generic NameOBTURATOR
Product CodeCAO
Date Received1999-10-20
Returned To Mfg1999-10-01
Model NumberETO-CFR25
Catalog NumberETO-CFR25
Lot NumberCZ (3/96)
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key238826
ManufacturerCIRCON ACMI
Manufacturer Address93 NORTH PLEASANT ST. NORWALK OH 448570409 US
Baseline Brand NameUSA ELITE CFR TIMBERLAKE OBTURATOR
Baseline Generic NameOBTURATOR
Baseline Model NoETO-CFR25
Baseline Catalog NoETO-CFR25
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 1999-10-20

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