45 results · 21ms · Sources: EU EUDAMED, US FDA

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HICP200 Patient/Monitor Interconnect Cable

FDA 510(k)
FDA Class 2 ·Neurology

XENMATRIX

FDA UDI
Davol Inc.·00801741074370·XenMatrix Surgical Graft, 10 cm x 10 cm (3.9" x...

OSS™ Orthopedic Salvage System

FDA UDI
Biomet Orthopedics, LLC·00880304250758·

HAMILTON-MR1

FDA UDI
Hamilton Medical AG·07630002800761·

MEGA SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809763500558·Mono Screw Driver

Mui Scientific

FDA UDI
H & A Mui Enterprises Inc·10678467505412·CUSTOMIZED SINGLE-USE ANTRODUODENAL 16CH CATHETER

Vilex Power Accessory

FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)

FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL: KD-5963NU, KD-5008

FDA 510(k)
FDA Class 2 ·Cardiovascular

FUTURE MOBILITY HEALTHCARE INC. ORION II WHEELCHAIR AND STELLATO MECHANICAL WHEELCHAIR

FDA 510(k)
FDA Class 1 ·Physical Medicine

eTRAX™ Needle

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436103371·Sterile needle, 16GA x 10cm with (7.6 tapered t...

Compression Staple System

FDA UDI
TORNIER, INC.·00846832055128·Staple

OSS REINFORCED YOKE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·March 21, 2023

OSS CEMENTED IM STEM 15X225

FDA Adverse Event
Injury ·.·Product code JDI·March 21, 2023

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

LOCKING BLUNT CANNULA, 11 GAUGE

FDA Adverse Event
Malfunction ·CAREFUSION CORPORATION·Product code FPA·July 23, 2014

UNICEL DXC 800 SYNCHRON SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·June 17, 2011

Hamilton-MR1, REF: 161010, Intensive Care Ventilator

FDA Recall
Open, Classified ·Hamilton Medical, Inc.·Product code CBK·July 26, 2023

Hamilton-MR1, REF: 161010, Intensive Care Ventilator

FDA Enforcement
Class I ·Ongoing·Hamilton Medical, Inc.·September 27, 2023

LATITUDE ELBOW ANATOMIC HUMERAL SPOOL SZ PETIT+ SIDE DROIT

FDA Adverse Event
Injury ·TORNIER INC·Product code JDB·September 20, 2024

BIODESIGN OTOLOGIC REPAIR GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code KHJ·September 19, 2018