Device Recall Transseptal Sheath Introducer Kits

  • Modèle / numéro de série
    Catalog Numbers: XD252500, XD252501, XD252502, XD252503, XD252504, XD252505, XD252506, XD252507, XD252508, XD252509, TF8-38-62-5, TF8-38-62-B1, FCL-127-00, FCL-127-01, FCL-127-02, FCL-127-03, FCL-127-04, FCL-127-05, FCL-127-06, FCL-127-07, FCL-127-08 and FCL-127-09; and  Lot Numbers: 25346, S20361, S20361X1, S20362, S20362X1, S20452, S20501, S20501X1, S20502, S20502X1, S20503, S20504, S20971, S20980, S21218, S21218X1, S21244, S21270, S21270X1, S21271, S21272, S21273, S21278, S21571, S21828, S21903, S21904, S21905, S21906, S21940, S21973, S22005, S22019, S22020, S22057, S22088, S22094, S22095, S22096, S22107, S22108, S22235, S22236, S22237, S22237X1, S22238, S22239, S22240, S22241, S22242, S22243, S22246, S22495, S22496, S22497, S22498, S22598, S22613, S22614, S22670, S22677, S22739, S22739X1, S22754, S22871, S22880, S22890, S22908, S22939, S22950, S23012, S23163, S23380, S23400, S23401, S23449, S23454, S24213, S24759, S25171, S25393, S25536, S25618 S25647, S26047, S26129, S26480, S26969, S26970, S27089, S27367, S27368, S27369, S27466, S27587, S27631, S27632, S27647, S27767, S27768, S27772, S27953, S27966, S28055, S28539, S28555, S28587, S28796, S29034, S29035, S29527, S29659, S29660, S29934, S30137, S30427, S30428 and S30519.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- United States (CA, MA and NJ), Canada, Germany, and the United Kingdom.
  • Description du dispositif
    Transseptal Sheath Introducer Kits (under trade names: HeartSpan, Channel FX, Torflex, Braided Guiding Introducer Kit). The product is shipped 5 per carton. || Intended to allow left heart catheterization procedure to occur through the right atrium.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Thomas Medical Products Inc, 65 Great Valley Pkwy, Malvern PA 19355-1302
  • Source
    USFDA