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

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    Ophthlamic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·10841668115159·BARRAQUER SPECULUM Disposable with Finger tabs ...

    In-Ka Ureteral Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Zavation

    FDA UDI
    Zavation LLC·00842166132030·Ti3Z CIF 12mmx14mmx7mm -10 deg

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540430083·HAEMOSTATIC FCPS,HALSTEAD-MOSQUITO,CVD.

    TALOS®-C HA

    FDA UDI
    MEDITECH SPINE, LLC·B167522010070·

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869634526·MOSS VRS rod rotation key

    NA

    FDA UDI
    Biedermann Motech GmbH & Co. KG·04250869691666·MOSS VRS MIS XT rod rotation key straight, 1/4"...

    PROFEMUR GLADIATOR Thin HA Classic Hip Stem with Collar

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ULTRA PRESERVE WITH ALOE VERA (GREEN) NATURAL RUBBER LATEX EXAMINATION GLOVE MADE FROM ALLOTEX AN ENZYME TREATED NATURAL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    BIOM PACK, Contents Individually Sterile. QTY 5 EA. Each Pack Contains: 1 EA. Microscope Drape (REF40100), 1 EA. Cornea Coat (REF 60010), 1 EA. SuperView BIOM Lens Set (REF 40411). Manufactured by: Insight Instruments, Inc., 2580 SE Willoughby Blvd. Stuart, FL 34994 USA. Item # 40201: Item Lot # Cornea Coat Lot # Expiration Date M423801008 M419300908 2010-07 M427731108 M419300908 2010-07 M428631008 M419300908 2010-07 M434211208 M422951008 2010-08 M439670109 M422951008 2010-08 M443700109 M435381208 2010-09 M44887 M442120109 2010-10 Item # 40202: Item Lot # Cornea Coat Lot # Expiration Date M427641008 M419300908 2010-07 M45414 M435381208 2010-09 Item # 40203: M416600908 M415950808 2010-06 M422941008 M416620908 2010-07 M427651108 M422951008 2010-08 M442710109 M435381208 2010-09 M44870 M442120109 2010-10 Item # 40204: Item Lot # Cornea Coat Lot # Expiration Date M421580908 M416620908 2010-07 M435201208 M422951008 2010-08 M45645 M435381208 2010-09 Item # 40205: Item Lot # Cornea Coat Lot # Expiration Date M410510708 M409570708 2010-05 M412790708 M409570708 2010-05 M419280908 M415950808 2010-06 M420850908 M415950808 2010-06 M421100908 M416620908 2010-07 M421120908 M416620908 2010-07 M424361008 M419300908 2010-07 M425821008 M421680908 2010-07 M426731008 M421680908 2010-07 M428601008 M419300908 2010-07 M429531108 M421680908 2010-07 M430851108 M421680908 2010-07 M431051108 M422951008 2010-08 M433111108 M422951008 2010-08 M435531208 M430041108 2010-09 M440700109 M430041108 2010-09 M441790109 M435381208 2010-09 M442560109 M430041108 2010-09 M443450109 M422951008 2010-08 M443930109 M442120109 2010-10 M44605 M442120109 2010-10 M44896 M44499 2010-11 M45099 M44499 2010-11 M45243 M435381208 2010-09 M45248 M44897 2010-12 M45866 M44897 2010-12 M45870 M435381208 2010-09 Item # 10206: Item Lot # Cornea Coat Lot # Expiration Date M418460908 M416620908 2010-07 M434741208 M422951008 2010-08 M45646 M435381208 2010-09

    FDA Recall
    Terminated ·Insight Instruments, Inc.·Product code KYG·May 12, 2010

    BD PLASTIPAK¿ PLASTIC CONCENTRIC LUER-LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 22, 2022

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE LTD·Product code FRN·October 20, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 2, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·November 28, 2023

    ANCHOR PLATE,STANDARD,T-SHAPE,SHORT

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code DZE·February 5, 2018

    BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Recall
    Open, Classified ·Stryker Sustainability Solutions·Product code NLH·April 10, 2026

    ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot 4401214, Use Before 2010-07.

    FDA Recall
    Terminated ·Product code NIP·April 9, 2008