28 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OXIMAX N-550 PULSE OXIMETER,MODEL N-550 PULSE OXIMETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Sterile Specimen Container
FDA UDI
Thermo Fisher Scientific (Monterrey), S. de R.L. de C.V.·17503025060092·90ML/53MM SPC W/LBL, OR CP, ST
Samco™ Bio-Tite™ Wide Mouth, ST 90mL, 53mm, w/lab, ORG Cap
FDA UDI
Nalge Nunc International Corporation·10850016060492·90ML/53MM SPC W/LBL, OR CP, ST
Pitch-Patch 30 mm x 20 mm
FDA UDI
XIROS LTD·05060267132017·
AOS ANTI-ROTATION SCREW 5.0mm x 90mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665019902·
Pitch-Patch 30 mm x 20 mm
FDA UDI
XIROS LTD·05060267133755·
Reicodent
FDA UDI
devemed GmbH·04061644052288·Needle holder "Derf" | 12 cm
straight
TC, 4-0 -...
CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
METHAFILCON A
FDA 510(k)
FDA Class 2
·Ophthalmic
CONTAINER SPECIUM
FDA Adverse Event
Other
·FISHER SCIENTIFIC·Product code NNI·April 27, 2017
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code DYB·April 11, 2025
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·October 21, 2020
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·April 8, 2025
INTROCAN SAFETY®
FDA Adverse Event
Injury
·B BRAUN MELSUNGEN AG·Product code FOZ·April 1, 2025
35 CM BIPOLAR LEAD
FDA Adverse Event
Malfunction
·GREATBATCH MEDICAL·Product code DTB·March 20, 2013
SPRINT FIDELIS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011
INTRATHECAL CATHETER
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·March 27, 2008
INTROCAN SAFETY®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FOZ·March 20, 2025
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·April 1, 2021
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·April 1, 2021