28 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DANA EMULATING INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
SCHWARTZ VESSEL CLIP
FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008910·SCHWARTZ VESSEL CLIP ANGLED
ABR / ASSR Lead Cable Set
FDA UDI
PATH medical GmbH·04260223143724·Electrode lead cables
(use with trunk cable) cr...
NITANIUM® ARCHWIRES
FDA UDI
Ortho Organizers, Inc.·00190707065799·.019 X .025 Lower Coated Nitanium® Pro Form™ Ar...
ABR / ASSR Lead Cable Set
FDA UDI
PATH medical GmbH·04260223143328·ABR / ASSR electrode lead cable set
Portex
FDA UDI
ICU MEDICAL, INC.·15019315065965·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315066177·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315042676·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315069345·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315042683·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315106880·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315042690·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315106873·
Portex
FDA UDI
ICU MEDICAL, INC.·15019315106897·
MODIFICATION TO HYBRID CAPTURE II CT/GC TEST, MODEL 03M90-01
FDA 510(k)
FDA Class 1
·Microbiology
STERILE LATEX POWDERED PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·February 6, 2018
Widex
FDA UDI
Widex A/S·05706069773545·Widex EVOKE E-FA (Lime Green S-110 ) Telecoil, ...
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2013
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·September 19, 2014