Manufacturers

Allen Medical Systems

2 devices in the database

Device Recall Allen Medical
  • Model / Serial
    Serial Numbers:  260227 260228 260229 260230 262208 A032121 A032122 A032123 A032124 A032125 A032126 A032128 A032129 A032340 A032942 A032944 A033038 A033039 A033040 A033920 A033921 A033922 A033923 A033924 A033925 A033927 A033928 A033929 A034241 A034242 A034243 A034623 A034624 A034626 A034627 A034628 A034877 A034907 A034909 A035239 A035242 A035243 A035623 A035624 A035625 A037489 A040087 A040359 A040360 A040361 A040362 A040363 A040364 A040650 A040693 A040694 A040778 A040779 A040780 A040781 A040782 A041742 A041743 A041744 A041745 A041746 A041747 A042080 A042081 A042082 A042159 A042533 A042534 A042640 A042641 A043683 A043684 A043953
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Foreign: Australia, Greece, Italy, Ireland
  • Product Description
    Allen A-91000 Shoulder Positioner
Device Recall AMATECH
  • Model / Serial
    131613, 131614, 131615, 131616,152144, 152145, 152147, 152148 219039, 219040, 219042, 219043, 232800, 232801, 232802, 232803, 232804, 205395, 205396, 235327, 235329, 235330, 237473, 237465, 237467, 237468, 237469, 237470, 237471
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    SC
  • Product Description
    Neuro Adapter 2 used with the Berchtold B-810 Surgical Table or Getinge USA Fortis Surgical Table || Catalog No: MDTNA2

9 manufacturers with a similar name

Learn more about the data here

Allen Medical Systems Inc
Allen Medical Systems, Inc.
  • Manufacturer Address
    Allen Medical Systems, Inc., One Post Office Square, Acton MA 01720
  • Manufacturer Parent Company (2017)
    Hill-Rom Holdings, Inc
  • Source
    USFDA
Allen Medical Systems
  • Manufacturer Address
    Allen Medical Systems, 100 Discovery Way, Acton MA 01720-4481
  • Manufacturer Parent Company (2017)
    Hill-Rom Holdings, Inc
  • Source
    USFDA
ALLEN MEDICAL SYSTEMS, INC.
  • Manufacturer Parent Company (2017)
    Hill-Rom Holdings, Inc
  • Manufacturer comment
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
ALLEN MEDICAL SYSTEMS Inc.
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