21 results · 20ms · Sources: EU EUDAMED, US FDA

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REPROCESSED STEERABLE INTRODUCER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SBH

FDA UDI
SBH Surgical·00850068304011·1/1, Sterilization Container Perforated Lid, Bl...

ArgenZ ST 98x12 ML A3.5

FDA UDI
ARGEN CORPORATION, THE·D818123334·Dental porcelain/ceramic restoration kit

RUSCH

FDA UDI
TELEFLEX INCORPORATED·04026704541775·PVC NASOPHARYNGEAL AIRWAY STERILE

Novo Surgical Inc.

FDA UDI
NOVO SURGICAL, INC.·00842331169427·sterile surgical blades, box of 100 blades, no. 23

CARDIO MED

FDA 510(k)
FDA Class 2 ·Cardiovascular

BMC CATHETER CONNECTOR CABLE, MODEL RFP-101

FDA 510(k)
FDA Class 2 ·Cardiovascular

EASYSPINE SCREW, UNKOWN SIZE OR TYPE

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·August 17, 2020

LINER: VERSAFITCUP CC TRIO FLAT PE HC LINER Ø 28 / B

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 31, 2024

BD NEXIVA¿ DIFFUSICS¿ CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·July 22, 2022

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

MICRO SAGITTAL SAW

FDA Adverse Event
Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·June 8, 2011

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE ROD, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE SCREW, UNKNOWN

FDA Adverse Event
Injury ·LDR MEDICAL·Product code NKB·March 24, 2020

EASY SPINE ROD, UNKNOWN

FDA Adverse Event
Malfunction ·LDR MEDICAL·Product code NKB·March 24, 2020

EASYSPINE SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·LDR MÉDICAL·Product code NKB·July 9, 2019