45 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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