422 results · 23ms · Sources: EU EUDAMED, US FDA

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SAFECARE Multi-Drug Urine Test Cup, SAFECARE Multi-Drug Urine Test Dip Card

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

OIC Pedicle Screw System

FDA UDI
ORTHOPAEDIC IMPLANT COMPANY, THE·M69622011200·COMPRESSOR

Pantheon System

FDA UDI
ADLER ORTHO SPA·08050880238316·Pantheon Bridging Collar Ø 30 mm for Stem Ø 12 mm

OsteoMed

FDA UDI
OSTEOMED LLC·00845694019453·2.0mm Screwdriver Shaft, Manual

MULTI-GUIDE

FDA UDI
Stryker Leibinger GmbH & Co. KG·04546540257758·HANDLE FOR DRILL GUIDE

VICEROY Spinal System

FDA UDI
EOS BIOTEK,INC.·88000163011828·

Viceroy

FDA UDI
DIOMEDICAL CO.,LTD.·08800039826211·Rod 6.0 x 120mm

ENVOY PATIENT MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

RADIAL ARTERY CATHERIZATION SET WITH INTEGRAL NEEDLE PROTECTION,MODEL RA-04020-SP

FDA 510(k)
FDA Class 2 ·Cardiovascular

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE CANADA LTD.·Product code MMI·August 2, 2011

SPRINT FIDELIS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 13, 2011

ENTRUST AT

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·October 13, 2011

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 4, 2012

ENTRUST AT

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·August 11, 2011

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·October 6, 2011

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE CANADA LTD.·Product code MMI·August 31, 2011

I-STAT TROPONIN (CTNI) CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE CANADA LTD.·Product code MMI·September 2, 2011

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 11, 2011

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 2, 2013