7,399 results
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32ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Guide
FDA UDI
Osstem Implant Co., Ltd.·08809892361136·
Guide
FDA UDI
Osstem Implant Co., Ltd.·08800000979656·
ETNIA EYEWEAR CULTURE
FDA UDI
Etnia Barcelona, Llc.·08435736023054·Sunglasses (non-prescriptionincluding photosens...
ETNIA EYEWEAR CULTURE
FDA UDI
Etnia Barcelona, Llc.·08435736023047·Frame Spectacle
SEPARATOR, AUTOMATED, BLOOD CELL AND PLASMA, THERAPEUTIC
FDA Adverse Event
Death
·UNK·Product code LKN·December 3, 2020
PLASMAPHERESIS
FDA Adverse Event
UNK·Product code LKN·December 3, 2020
PLASMAPHERESIS
FDA Adverse Event
Injury
·UNK·Product code LKN·December 3, 2020
EVIS EXERA III COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDF·July 20, 2023
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·March 14, 2023
OPRA IMPLANT SYSTEM
FDA Adverse Event
Injury
·INTEGRUM AB·Product code PJY·February 6, 2020
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·November 18, 2022
BD PYXIS¿ MEDSTATION¿ ES AUXILIARY
FDA Adverse Event
Malfunction
·CAREFUSION 303, INC.·Product code BRY·March 30, 2026
HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·May 28, 2021
TISSUE-TEK VIP(R)5 VACUUM INFILTRATION PROCESSOR FLOOR 230 V, 50 HZ
FDA Adverse Event
Injury
·SAKURA FINETEK USA, INC.·Product code IEO·February 2, 2018
AXIOM LUMINOS DRF
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE GMBH·Product code OWB·November 4, 2022
Caudal Anesthesia Kit
FDA classification
FDA Class 2
·Caudal Anesthesia Kit
OEB S.R.L.
FDA registration
OEB S.R.L.·22 products·🇮🇹 Italy
OGI, LLC
FDA registration
OGI, LLC·3 products·🇺🇸 United States
TrueLabor Monitor Adapter
FDA UDI
O.B - TOOLS LTD·07290016406023·The TrueLabor's Monitor Adapter for the hospita...
TrueLabor Maternal Unit
FDA UDI
O.B - TOOLS LTD·07290016406016·TrueLabor's Maternal Unit is connected via a pr...