767 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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APNEALINK PRO
FDA 510(k)
FDA Class 2
·Anesthesiology
Bernafon
FDA UDI
Bernafon AG·05711584050156·PC9 CPX, VC PS BE PRECISO 9
K131982
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·February 23, 2024
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414468·Orthopaedic prosthesis instrument, reusable - G...
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365432·Femoral head prosthesis trial - General instrument
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365401·Femoral head prosthesis trial - General instrument
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414499·Orthopaedic prosthesis instrument, reusable - G...
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414475·Orthopaedic prosthesis instrument, reusable - G...
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575414482·Orthopaedic prosthesis instrument, reusable - G...
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365425·Femoral head prosthesis trial - General instrument
LINK Instruments - Trial implants and size gauges
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575365418·Femoral head prosthesis trial - General instrument
FLUORIDE VARNISH
FDA 510(k)
FDA Class 2
·Dental
IGLUCOSE SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·May 29, 2013
SWAN-GANZ CCOMBO CCO/SVO2/VIP THERMODILUTION CATHETER WITH AMC THROMBOSHIELD
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES, PR·Product code DYG·June 16, 2011
ZENITH AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK, INC.·Product code MIH·August 22, 2008
BIPAP PRO BIFLEX
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code BZD·March 2, 2026
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·July 21, 2021
DREAMSTATION BIPAP AUTOSV
FDA Adverse Event
Malfunction
·RESPIRONICS, INC·Product code MNS·March 30, 2022