17 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REVITIVE IX
FDA 510(k)
FDA Class 2
·Physical Medicine
ArgenZ ST 98x14 ML B4
FDA UDI
ARGEN CORPORATION, THE·D818123354·Dental porcelain/ceramic restoration kit
Logical G-Series Acetabular Shell
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215052133·
Paxeon Logical
FDA UDI
PAXEON RECONSTRUCTION LLC·08177570201273·Logical G-Series Shell – 3 Holes Size 54-C
Logical G-Series
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215000882·
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111233540·54mm Acetabular Cup (3-hole)
COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81E
FDA 510(k)
FDA Class 2
·Anesthesiology
EBONY PTA .035 PERIPHERAL DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
VENTO Cup
FDA UDI
AMPLITUDE SAS·03701089514064·
BD PEN NEEDLE¿ 31GX5MM 7 PACK
FDA Adverse Event
Injury
·BD (SUZHOU)·Product code FMI·April 1, 2019
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
NEXIVA DIFFUSICS
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 30, 2026
BD MICRO-FINE¿ PEN NEEDLE
FDA Adverse Event
Injury
·BD (SUZHOU)·Product code FMI·May 8, 2019
PEN NEEDLE 31GX5MM 7 PACK
FDA Adverse Event
Injury
·BD (SUZHOU)·Product code FMI·March 29, 2019
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
TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code HCG·June 14, 2011