BEUDAMED
    33 results · 17ms · Sources: EU EUDAMED, US FDA

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    BD, Proteus Polyvalent Antiserum (OXK, OX2, OX19)

    FDA Recall
    Terminated ·BD Diagnostic Systems·Product code GSY·October 20, 2004

    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    J-VAC Reservoir is a component of the J-VAC Closed Wound Drainage System. This system is a sterile, portable system used for closed wound drainage. This system is composed of two parts: the J-VAC Reservoir and Suction Drains.

    FDA Recall
    Terminated ·Ethicon, Inc US·Product code GCY·August 31, 2005

    Blood Gas and Co-Ox2 Electrolyte & Metabolyte Analyzers, ABL-700 Series, manufactured from 8/1998 through 11/2004.

    FDA Recall
    Terminated ·Radiometer America Inc·Product code JFP·September 29, 2005

    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances

    FDA Recall
    Completed ·STRATASYS LTD·Product code EBI·January 19, 2024

    IntelliVue Clinical Information Portfolio (ICIP) Critical Care Release D, Version D.02. Intended for use in data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. It is indicated for use by healthcare providers whenever there is a need for generation of a patient record and computation of drug dosage.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DXJ·October 21, 2009

    Spacelabs Model 91367 SL 2200 Compact Monitor Spacelabs Medical patient monitors passively display data generated from Spacelabs Medical patient parameter modules, Flexport interfaces, gas analyzers, and other SDLC based products.

    FDA Recall
    Terminated ·Spacelabs Healthcare, Incorporated·Product code DXJ·November 6, 2009

    Spacelabs Medical Flat Panel Display is a touchscreen display, 19-inch thin film transistor liquid crystal display (TFT-LCD). The PNs are 010-1619-00 and 010-1655-00, Models 94260-19 and 94256.

    FDA Recall
    Terminated ·Spacelabs Healthcare, Llc·Product code DXJ·March 20, 2009

    KODAK GP FLEXIBLE PHOSPHOR SCREENS, for use with Kodak DirectView CR 500 systems. Responsible firm on label: Made in U.S.A. by Eastman Kodak Company, Rochester, N.Y. 14650. Screens are sold in the following sizes and Cat. Nos: (1) Cat. #812-7334 - 15 x 30 cm; (2) Cat #825-9269 - 18 x 24 cm; (3) Cat #167-8663 - 24 x 30 cm; (4) Cat #810-7823 - 35 x 35 cm; (5) Cat #160-5906 - 35 x 43 cm

    FDA Recall
    Terminated ·Eastman Kodak Co·Product code IXJ·April 8, 2005

    Neoligaments Staple Impactor, 6 mm Staple Impactor: 202-3001

    FDA Recall
    Terminated ·Xiros Plc 28-30 Blenheim Terrace Leeds United Kingdom·Product code HXJ·May 17, 2006

    IntelliVue Clinical Information Portfolio Critical Care Release D, Version D.00.00 Product Number: 865047. This device is a clinical information system intended for use in data collection, storage, and management with independent bedside devices, and other systems that are connected either directly or through networks. It is used when there is a need for generating patient records and computation of drug dosage.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code DXJ·March 4, 2008

    Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A

    FDA Recall
    Open, Classified ·Product code DXJ·July 27, 2022

    Philips IntelliVue Clinical Information Portfolio Software Version D.0, for patient data collection, storage, and management.

    FDA Recall
    Terminated ·Philips Healthcare Inc.·Product code DXJ·May 5, 2009

    CareVue Chart Release C ,Versions C.00.00 through C.00.06 Product No. 862246. This device is a clinical information system intended for use in data collection, storage, and management with independent bedside devices, and other systems that are connected either directly or through networks. It is used when there is a need for generating patient records and computation of drug dosage.

    FDA Recall
    Terminated ·Philips Medical Systems·Product code DXJ·March 4, 2008

    Ultraview Universal Clinical Workstation System Model 90385.

    FDA Recall
    Terminated ·Spacelabs Medical Incorporated·Product code DXJ·January 7, 2005

    GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated), REF 2082278-001, and MAS700 (Desktop, REF 2082279-001.

    FDA Recall
    Open, Classified ·GE Healthcare, LLC·Product code DXJ·January 28, 2022

    Model: Description/REF: MNA-420: MNA-420 ENC -H/K9303320, MNA-420 DEC -H V2/K9303331; MNA-440: MNA-440 ENC -H/K9303300, MNA-440 DEC -H V2/K9303311; MNA-620: MNA-620 DEC -H/K9306210, MNA-620 ENC -H/K9306220; and MNA-640: MNA-640 DEC -H/K9306410, MNA-640 ENC -H/K9306420; components of the NexxisOR system

    FDA Recall
    Open, Classified ·Barco N.V. President Kennedypark 35 Kortrijk Belgium·Product code DXJ·May 9, 2025