Terumo Cardiovascular Systems Corporation

12 devices in the database

  • Model / Serial
    6912 , 6913 6914, 6932, 6933 6934, 6922, 6923 6924, CV-6912, CV-6913, CV-6914 Cardiovascular Procedure Kits- Various
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA (nationwide) Distribution.
  • Product Description
    CDI¿ H/S Cuvette || The intended use for the CDI¿ H IS Cuvette is as follows: The CDI¿ H/S Cuvettes are intended for use with a CDI monitor during cardiopulmonary bypass procedures when continuous monitoring of blood hematocrit and oxygen saturation is desired.
  • Model / Serial
    Serial Number Range 70194 through 70504
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Terumo Cardiovascular has identified 16 domestic consignees and 30 international consignees .
  • Product Description
    Hercules 360 Universal Stabilizing Arm, top mount, 360-degree rotation, reusable stainless steel
  • Model / Serial
    Catalog Number: 401-231, Product Description: Titan" Stabilizer Attachment , Lot Number: 052R   Catalog Number 401-231u , Product Description TitanTM 360 Stabilizer Attachment , Lot Number: 020R, 024R, 026R, 029R, 030R,034R,035R,037R, 040 , 048R
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    The product was distributed domestically and also to foreign consignees. But not to government agency's or Canada.
  • Product Description
    Titan" Stabilizer Attachment and Titan TM 360 Stabilizer || Attachment
  • Model / Serial
    TAOS, TC03
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Terumo CVS has identified 33 domestic consignees and 0 international consignee that are affected by this recall
  • Product Description
    The Sarns Centrifugal Pump is a single use device sterilized by ethylene oxide gas. The device is sold single sterile in cartons of 8 units, or may be provided in bulk, non-sterile to another Terumo location for inclusion in Cardiovascular Procedure Kits. Cardiovascular Procedure kits are packaged individually.
  • Model / Serial
    SAFETY ALERT Lot Codes:  (a) RH14, RK11, RK20, RL02, RM06, RM20, RN10, RP08, TD16, TE13, TE27, TF14, TF21, TG04, TG11, TG17, TH06, TH16, TK10, TK24, TL08, TL21, TM28, TP14, UA11, UA18, UA25, UC08, UC22, UD14, UD21, UD28, UE05, UE18, UF09, UG06, UK01, UL12, UM10, UM31, UP05, VA02, VC06, VD06, VE10    (b) RH14, RH21, RK18, RL15, RM01, RM22, RN24, RP01, TA19, TF05, TF27, TG19, TH20, TK24, TL01, TM12, TN09, TP03, UA20, UC15, UD22, UE04, UE18, UF02, UG13, UH11, UK15, UL06, UM10, VA02, VA30, VC27, VE03, VF01   LH130 PRODUCT CORRECTION lot codes or serial number range: TA19 through VD06, distribution date range: 08Apr2015 through 20Jan2017
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
  • Product Description
    TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J
7 more

13 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Rd, Ann Arbor MI 48103-9586
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Rd, Ann Arbor MI 48103
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
8 more