BEUDAMED
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    Brand Name: MST Duet Reusable Handle for Single Use Heads Product Name: Reusable Handle for Single Use Heads (Forceps and Scissors) Model/Catalog Number: DFH-1028 Software Version: N/A Product Description: A MST Single Use Forceps or Scissors System consists of a reusable handle and one of a number of single use interchangeable heads. MST Single Use Forceps and Scissor heads are shipped ready to use sterile in a tray with Tyvek lid within a sterile pouch. MST Duet Reusable Handle for Single Use Forceps & Scissor Heads are supplied in a non-sterile condition and must be sterilized prior to and after every use. The blue sleeve the handle is packaged in is not intended to be sterilized and does not maintain sterility. Component: Yes. The MST Duet Reusable Handle for Single Use Heads is the reusable handle component which connect to either Single Use Forceps or Scissors heads.

    FDA Recall
    Open, Classified ·MicroSurgical Technology Inc·Product code HNF·September 17, 2024

    MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01

    FDA Recall
    Open, Classified ·MicroSurgical Technology Inc·Product code HNN·August 20, 2025

    EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 14553901

    FDA Recall
    Open, Classified ·Phadia US Inc·Product code MST·May 1, 2023

    Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 12410002

    FDA Recall
    Open, Classified ·Phadia US Inc·Product code MST·May 1, 2023

    Microsurgical Operating Room Tables;7300BX (18-351-70).

    FDA Recall
    Open, Classified ·Mizuho America, Inc.·Product code GDC·September 11, 2019

    Microsurgical Operating Room Tables;7300B (18-350-70);

    FDA Recall
    Open, Classified ·Mizuho America, Inc.·Product code GDC·September 11, 2019

    Prelude IDEAL 4 F Hydrophilic Sheath Introducer, REF: PID4F16021PW/D

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DYB·January 27, 2025

    basixSKY Inflation Device, REF: SKY1802

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PTM·August 19, 2024

    MONARCH Inflation Device, REF: IN2430/B, IN2530/B, IN2130/B

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DXT·August 19, 2024

    Custom Waste Management Kit: REF: K10-00353K, K10-01603C, K10-01694Q, K10-05159B, K10-05743, K10-05825AP

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PPD·June 5, 2025

    Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DRE·August 12, 2024

    High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code FPK·June 5, 2025

    Blue Diamond Digital Inflation Device, REF: IN7152/C, IN7352/C, IN7403/C, IN7802/C, IN7852/C, IN7130/C

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DXT·August 19, 2024

    basixTOUCH Inflation Device, REF: IN8140/A

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PTM·August 19, 2024

    DiamondTOUCH Digital Inflation Device, REF: IN9135/A, IN9152/A

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DXT·August 19, 2024

    IntelliSystem Inflation Device, REF: IN1525/D

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code DXT·August 19, 2024

    Custom Procedure Kit, REF: K12T-11077

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code OEQ·August 12, 2024

    BlueFIRE Inflation Device, REF: IN10140

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PTM·August 19, 2024

    StabiliT TOUCH Syringe, REF: IN8VCF/B

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code OAR·August 19, 2024

    basixTOUCH Inflation Device, REF: IN8130/JPC, IN8152/C, IN8302/C, IN8352/C, IN8802/C, IN8130/C, IN8130/C

    FDA Recall
    Open, Classified ·Merit Medical Systems, Inc.·Product code PTM·August 19, 2024