10 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CUSTOMED LAP PACK IV
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HOTWIRE™ RF GUIDEWIRE
FDA UDI
Atraverse Medical, Inc·00850057445565·The HOTWIRE™ is a sterile, single-use guidewire...
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918116730·Alleset Gown_no reinforcement_XL/Xlong_35g SMS_...
Rampart One Lumbar Interbody Fusion System
FDA UDI
SPINEOLOGY INC.·M7404902031·Rampart One Trial, 16mm, M, 20°
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918160467·Alleset Gown_no reinforcement_XL/Xlong_w/ 2 Han...
VAPOR-CLEAR, MODEL 100
FDA 510(k)
FDA Class 2
·Anesthesiology
PHACOFRAGMENTATION SYSTEM MEGATRON
FDA 510(k)
FDA Class 2
·Ophthalmic
GEMSTR 7 THPY ALT ST
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 7, 2014
ASR UNI FEMORAL IMPL SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 8, 2013
ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·November 18, 2010