Manufacturers

Allen Medical Systems, Inc.

5 dispositifs dans la base de données

Device Recall Allen Medical CFlex, Polar Head Positioner Catalog Number A70700A1
  • Modèle / numéro de série
    Serial Numbers: A111211, A116292
  • Classification du dispositif
    Anesthesiology Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    MA, MS
  • Description du dispositif
    Allen Medical C-Flex, Polar Head Positioner || Catalog Number: A-70700-A1 || Product is a medical device used to maintain the position of an anesthetized patient during surgery.
Device Recall Ankle Traction Boot
  • Modèle / numéro de série
    A260264, A253312, A260989, A260262, 418292, A260991, A260998, A253313, A260993, A260265, 418293, A253309, A260995, A253310, A260992, A253311, 418294, A253323, A260261, A253321, A260994, 418291, 418295, A253322
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution- USA including the states of TX, NV, KY, GA, OH, PA, NY, AL, WA, IL and the countries of New Zealand and Japan.
  • Description du dispositif
    Allen Traction Boot, Modular, OT 1000 Traction Device Boot Assembly, Fracture Table Orthopedic Leg Holders, non-invasive medical devices designed to attach to orthopedic fracture tables to aid clinical staff in applying traction to the leg of a patient during surgical procedures.
Device Recall Allen CFlex Head Positioner
  • Modèle / numéro de série
    A128573, A157480, A164957, A165624, A179587, A200505, A200508, A203121, A203123, A203124, A203126, A205717, A205730, A205731, A207969, A207970, A207971, A207973, A208274, A208275, A208277, A208278, A208932, A208933, A208934, A209578, A210915, A210916, A210917, A210919, A210920, A214252, A214253, A214254, A214255, A214256, A214582, A214583, A214584, A215498, A215489, A215499, A215500, A216459, A216460, A216461, A217594, A217595, A217596, A217597, A218945, A219496, A219623, A219624, A220031, A220032, A220033, A220664, A220665, A222121, A222122, A222123, A222394, A223961, A223962, A223963, A223964, A224084, A224085, A224144, A224145, A225106, A225107, A225553, A225554, A22555, A225972, A225973, A226214, A226215, A226216, A226217, A226218, A226910
  • Classification du dispositif
    Anesthesiology Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- USA (nationwide ) and the countries of Africa, Australia, Bulgaria, China, Germany, India, Istanbul, France, Greece, New Zealand, Saudi Arabia,Singapore, Spain, Taiwan and Japan.
  • Description du dispositif
    Allen C-Flex Head Positioning System non-invasive medical device used to support a patient's head during spine surgery || Catalog Numbers: A-70700 and A-70701-2
Device Recall Arthrex Shoulder Suspension Tower
  • Modèle / numéro de série
    Serial Numbers: 501798, 501799, 501800, 501801, 501802, 501803, 501804, 501805, 501806, 501807, 501808, 501809, 501810, 501811, 501812, 501813, 501814, 501815, 501816, 501817, 501818, 501819, 501820, 501821, 501822, 501823, 501824, 501825, 501826, 501827, 501828, 501829, 501830, 501831, 501832, 501833, 501834, 501835, 501836, 501837, 501838, 501839, 501840, 501841, 501842, 501848, 501849, 501850, 501851, 501852, 501853, 501854, 501855, 501856, 501857, 501863, 501864, 501865, 501866, 501867, 501868, 501869, 501870, 501871, 501872, 501878, 501879, 501880, 501881, 501882, 501883, 501884, 501885, 501886, 501887, 501888, 501889, 501890, 501891, 501892, 501893, 501894, 501895, 501896, 501897, 510733, 510734, 510735, 510736, 510737, 510738, 510739, 510740, 510741, 510742, 510743, 510744, 510745, 510746, 510747, 510748, 510749, 510750, 510751, 510752, 510834, 510835, 510836, 510837, 510838, 510839, 510840
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    US state of FL
  • Description du dispositif
    Arthrex Shoulder Suspension Tower; Catalog Number: AR-1650-01 || Product Usage: || The Arthrex Lateral Decubitus Shoulder Positioner is intended to allow for the controlled manipulation of the arm and shoulder joint during arthroscopic surgical procedures.
Device Recall Arthex S3 Arm Sleeve Connector
  • Modèle / numéro de série
    499633 499694 499274 499367 499410 499383 499479 499573 499615 499634 499695 499275 499368 499411 499384 499480 499574 499616 499635 499696 499276 499369 499412 499385 499481 499575 499617 499636 499697 499277 499370 499413 499386 499482 499576 499618 499637 499698 499278 499371 499414 499387 499483 499577 499619 499638 499699 499279 499372 499415 499388 499484 499578 499620 499639 499700 499280 499323 499416 499389 499485 499579 499621 499640 499701 499281 499324 499417 499390 499486 499580 499622 499641 499702 499282 499325 499418 499391 499487 499581 499623 499659 499703 499283 499326 499419 499392 499488 499582 499624 499660 499704 499284 499327 499420 499393 499471 499583 499625 499661 499705 499285 499328 499421 499394 499472 499584 499626 499662 499706 499286 499329 499422 499395 499489 499585 499627 499663 499707 499287 499330 499423 499396 499490 499586 499628 499664 499708 499288 499331 499424 499397 499491 499587 499629 499665 499709 499289 499332 499425 499440 499492 499588 499630 499666 499710 499290 499333 499426 499441 499493 499589 499552 499667 499298 499291 499334 499427 499442 499494 499590 499553 499668 499299 499292 499335 499428 499443 499495 499592 499554 499669 499300 499293 499336 499429 499444 499496 499593 499555 499671 499301 499294 499337 499430 499445 499497 499594 499556 499672 499302 499295 499338 499431 499446 499498 499595 499557 499673 499303 499296 499339 499432 499447 499499 499596 499558 499674 499304 499297 499340 499433 499448 499500 499597 499559 499675 499305 499348 499341 499434 499449 499501 499598 499560 499676 499306 499349 499342 499435 499450 499502 499599 499561 499677 499307 499350 499343 499436 499451 499503 499600 499562 499678 499308 499351 499344 499437 499452 499504 499601 499563 499679 499309 499352 499345 499438 499453 499505 499602 499564 499680 499310 499353 499346 499439 499454 499506 499603 499565 499681 499311 499354 499347 499468 499455 499507 499604 499566 499682 499312 499355 499398 499469 499456 499508 499605 499567 499683 499313 499356 499399 499470 499457 499509 499606 499568 499684 499314 499357 499400 499373 499458 499510 499607 499569 499685 499315 499358 499401 499374 499459 499511 499608 499570 499686 499316 499359 499402 499375 499460 499512 499609 499571 499687 499317 499360 499403 499376 499461 499473 499610 499538 499688 499318 499361 499404 499377 499462 499474 499611 499539 499689 499319 499362 499405 499378 499463 499475 499612 499540 499690 499320 499363 499406 499379 499464 499476 499631 499541 499691 499321 499364 499407 499380 499465 499477 499632 499542 499692 499322 499365 499408 499381 499466 499478 499613 499543 499693 499273 499366 499409 499382 499467 499572 499614 499544
  • Classification du dispositif
    Neurological Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    US Distribution to the state of : FL
  • Description du dispositif
    Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.

3 fabricants avec un nom similaire

En savoir plus sur les données ici

ALLEN MEDICAL SYSTEMS, INC.
  • Société-mère du fabricant (2017)
    Hill-Rom Holdings, Inc
  • Commentaire du fabricant
    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.
ALLEN MEDICAL SYSTEMS, INC.