12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Unity Subcutaneous Infusion System for Remodulin
FDA 510(k)
FDA Class 2
·General Hospital
Edge™ Diamond PMI010-3M Pear Minimally Invasive
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002714·Diamond dental bur, reusable
Bernafon
FDA UDI
Bernafon AG·05711584086148·ZR1 MNR T, 2.4G NFM DPB SABE/MSIL DEMO ZERENA 1
Orthos
FDA UDI
ORMCO CORPORATION·00889989030020·ORTHOS CM SST ARCH 021X025 LOLG PK10
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199038·AK3 Congruent Insert Trial Size 3, 13mm
EXSEPT SKIN AND WOUND CLEANSER WITH ANTIMICROBIAL PRESERVATIVE
FDA 510(k)
FDA Class 2
·General Hospital
SYSMEX MODEL XT-4000I
FDA 510(k)
FDA Class 2
·Hematology
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 26, 2013
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·July 28, 2011
LIFEPAK CR PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·September 26, 2008
MICROVASCULAR PLUG
FDA Adverse Event
Injury
·REVERSE MEDICAL·Product code KRD·September 8, 2021
MICROVASCULAR PLUG
FDA Adverse Event
Injury
·REVERSE MEDICAL·Product code KRD·September 8, 2021