BEUDAMED
    22 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    MICRORING YT

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Prehma

    FDA UDI
    Keystone Industries·H66819001121·MATRIX ROLL 3/16 0.015 ( BX X 10FT )

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746097089·DB BRACKET MASTER SERIES IBD MAND LEFT CUSPID 0...

    Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746099038·DB BKT MASTER LR CUSP 018 T-11 A+7 R2M

    Para-Pak LV-PVA

    FDA UDI
    MERIDIAN BIOSCIENCE, INC.·00840733103315·This DI Number represents the DI number on the ...

    Barricade Coil System

    FDA UDI
    BALT USA LLC·00818053021114·Barricade Coil System (BCS) is intended for the...

    3M™ Silvercel™

    FDA UDI
    3M Deutschland GmbH·25032749039446·3M™ Silvercel™ Non-Adherent Antimicrobial Algin...

    3M™ Unitek™

    FDA UDI
    3M COMPANY·30605861026971·3M™ Unitek™ Stainless Steel First Primary Molar...

    Para-Pak LV-PVA

    FDA UDI
    MERIDIAN BIOSCIENCE, INC.·00840733102448·Para-Pak / Para-Pak Ultra based systems provide...

    SILVERCEL

    FDA UDI
    ADVANCED MEDICAL SOLUTIONS LIMITED·15051978002499·14-24APX LAM Silver Hydro-Alginate NA

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930790011220·Custom Suction Nerve Root Retractor 8mm

    CONLIN MOLAR BAND

    FDA UDI
    Ortho Arch Company Inc·D90990011210·MOLAR BAND CONLIN RX UPPER RIGHT 34 1/2

    ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401

    FDA 510(k)
    FDA Class 1 ·Dental

    MIDAS REX MR7 PNEUMATIC HIGH SPEED SYSTEM, MODELS PM700, PM710, PC700, PC710, PC720, PA700

    FDA 510(k)
    FDA Class 2 ·Neurology

    Intervertebral Body Fusion Device

    FDA UDI
    PRECISION SPINE, INC.·00840019922814·Shaver 12mm

    ADULT BREATHING CIRCUIT DUAL HEATED

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTT·June 15, 2007

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·October 26, 2023

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 7, 2013

    6 SHOOTER SAEED MULTI-BAND LIGATOR

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code MND·October 22, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 28, 2014