Devices

Device Recall Surgical Bur

  • Modèle / numéro de série
    OEM Catalog number A-CRN-S.
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange 2.15MMX22MM Fluted Spiral Router for CRANI-A; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number A-CRN-S; || EXP (repackager), Anspach (OEM) || Bur, surgical, general & plastic surgery
  • Manufacturer
    EXP Pharmaceutical Services Corp
  • 1 Event

Fabricant

EXP Pharmaceutical Services Corp
  • Adresse du fabricant
    EXP Pharmaceutical Services Corp, 48021Warm Springs Boulevard, Fremont CA 94539
  • Société-mère du fabricant (2017)
    Abry Partners Inc.
  • Source
    USFDA

4 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

Device Recall Surgical bur
  • Modèle / numéro de série
    OEM Catalog number 5820-10-120.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange Round Fluted Bur Soft Touch; 2.0mm; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 5820-10-120; || EXP (repackager), Stryker (OEM) || Drills, burrs, trephines & accessories || (simple, powered)
  • Manufacturer
    EXP Pharmaceutical Services Corp
Device Recall Surgical bur
  • Modèle / numéro de série
    OEM Catalog number 5820-10-130.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange Round Diamond Bur Extra Coarse; 3.0mm; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 5820-10-130; || EXP (repackager), Stryker (OEM) || Drills, burrs, trephines & accessories || (simple, powered)
  • Manufacturer
    EXP Pharmaceutical Services Corp
Device Recall Surgical bur
  • Modèle / numéro de série
    OEM Catalog number 5820-10-160.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange 6.0mm Round Fluted Bur Soft Touch; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 5820-10-160; || EXP (repackager), Stryker (OEM) || Drills, burrs, trephines & accessories || (simple, powered)
  • Manufacturer
    EXP Pharmaceutical Services Corp
Device Recall Surgical bur
  • Modèle / numéro de série
    OEM Catalog number 5820-10-240.
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in DC and the states of CO, CA, FL, TX, and AR.
  • Description du dispositif
    Medical Device Exchange Round Fluted Bur Aggressive; 4.0mm; || Pouch, Tyvek/Mylar, Sterile, Single Use Only; || OEM Catalog number 5820-10-240; || EXP (repackager), Stryker (OEM) || Drills, burrs, trephines & accessories || (simple, powered)
  • Manufacturer
    EXP Pharmaceutical Services Corp