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Crédits
Devices
Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Lot code WFLV
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial; || Size 2 Left || Non-Sterile || Catalog Number 5512-T-201 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
Rappel de Device Recall Triathlon TS Femoral Trial
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Fabricant
Stryker Howmedica Osteonics Corp.
Adresse du fabricant
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
Société-mère du fabricant (2017)
Stryker
Source
USFDA
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Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Lot codeL WFLD
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial; || Size 1 Left || Non-Sterile || Catalog number 5512-T-101 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Lot Code WFLI
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial; || Size 1 Right || Non-Sterile || Catalog number: 5512-T-102 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Lot Code TYHMPD, WFCP.
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial; || Size 2 Right || Non-Sterile || Catalog Number: 5512-T-202 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Code Numbers N4TMPD, PDAMPD, WEWC
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial; || Size 3 Left || Non-Sterile || Catalog Number: 5512-T-301 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
Modèle / numéro de série
Lot Code: WFIC
Classification du dispositif
Orthopedic Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Description du dispositif
Triathlon TS Femoral Trial || Size 3 Right || Non-Sterile || Catalog Number : 5512-T-302 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
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