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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BIEDERMANN MOTECH GMBH &CO. KG TELIX K; 209-010-0502

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BIEDERMANN MOTECH GMBH &CO. KG TELIX K; 209-010-0502 Back to Search Results
Model Number 209-010-0502
Device Problem Accessory Incompatible (1004)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 05/10/2022
Event Type  malfunction  
Event Description
It was reported by the hospital, that both available set instruments from the telix k system jammed after the trials were inserted.After several attempts the instrument could be loosened from the trial and used to place the implant.The insertion of the implant worked without a problem.
 
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Brand Name
TELIX K
Type of Device
209-010-0502
Manufacturer (Section D)
BIEDERMANN MOTECH GMBH &CO. KG
bertha-von suttner str. 23
villingen-schwenningen, 78054
GM  78054
Manufacturer Contact
gerd federle
bertha-von-suttner strasse 23
villingen-schwenningen 78054
GM   78054
MDR Report Key14641313
MDR Text Key300467344
Report Number8010944-2022-00002
Device Sequence Number1
Product Code LXH
UDI-Device Identifier04250869633314
UDI-Public04250869633314
Combination Product (y/n)N
Reporter Country CodeSZ
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type User Facility
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 06/09/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/09/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number209-010-0502
Device Catalogue Number209-010-0502
Device Lot NumberBDM4WTG / BDM86TS
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer05/18/2022
Date Manufacturer Received05/18/2022
Was Device Evaluated by Manufacturer? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age51 YR
Patient SexMale
Patient EthnicityNon Hispanic
Patient RaceWhite
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