BEUDAMED
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    V-14 CONTROL WIRE GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017705·K-Wire, Double Ended, Trocar Point, Diameter Si...

    5550 1/2L SYRINGE

    FDA UDI
    HANS RUDOLPH, INC.·00874750009954·5550C 1/2L SYR 2in ID ORING OUTL

    TRIAGE TOX DRUG SCREEN, CATALOG #94000

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    HELICOBACTER PYLORI ELISA IGG TEST KIT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AGC DA2000 KN TIB BRG 71/75X8

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·April 9, 2026

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·May 14, 2013

    ISE INDIRECT NA+ FOR GEN.2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·June 3, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 15, 2008

    VANGUARD ROCC POR FEM S55 R

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·January 22, 2026

    VANGUARD ROCC POR FEM S57.5 L

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·January 22, 2026

    VANGUARD ROCC POR FEM S57.5 L

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBH·May 13, 2025

    TINBN VANGUARD INT PS ANAT FM R 75MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·June 4, 2025

    VANGUARD ROCC POR FEM S55 R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBH·June 4, 2025

    INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021

    Model Number L131, ESSENTIO DR EL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025