8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
artegral
FDA UDI
Merz Dental GmbH·D7091970247·anteriors; shade B4; mould IS
GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
Lacriflow CL
FDA 510(k)
FDA Unclassified
·Unknown
PALINDROME 28/45 KIT W/SLOT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code MSD·April 29, 2014
PERFUSOR SPACE
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·February 12, 2013
REPLY
FDA Adverse Event
Injury
·SORIN BIOMEDICA C.R.M., S.R.L.·Product code NVZ·January 14, 2011
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025