10,000 results
·
24ms
·
Sources: EU EUDAMED, US FDA
addition Junior/DIC Muster
Device
EU MDR
·
Eu Md Class 2a
·DETAX GmbH & Co. KG·On the market·32 countries
addition Junior DIC 80 x 50ml
Device
EU MDR
·
Eu Md Class 2a
·DETAX GmbH & Co. KG·On the market·32 countries
DIC TRACHEOSTOMY TUBE AND PORTEX BLUE LINE
FDA 510(k)
FDA Class 2
·Anesthesiology
addition Junior/DIC 4 x 50 ml
Device
EU MDR
·
Eu Md Class 2a
·DETAX GmbH & Co. KG·On the market·32 countries
addition Junior/DIC 2 x 50 ml
Device
EU MDR
·
Eu Md Class 2a
·DETAX GmbH & Co. KG·On the market·32 countries
addition Junior/DIC 4 x 50 ml
FDA UDI
DETAX GmbH·EDET041601·
addition Junior/DIC 2 x 50 ml
FDA UDI
DETAX GmbH·EDET041591·
OTOSONIC (OSI) LPS D; LPS D IC; LPS D ASP
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ABSORBABLE GELATIN
FDA Adverse Event
Injury
·PFIZER, INC.·Product code LMF·August 31, 2020
Edge™ Diamond DIC-016C Double Inverted Cone
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172007900·Diamond dental bur, reusable
Edge™ Diamond DIC-016C Double Inverted Cone
FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172007917·Diamond dental bur, reusable
DIC
FDA Adverse Event
Injury
·DALTON MEDICAL·Product code ITJ·October 18, 2010
MALLINCKRODT
FDA Adverse Event
Malfunction
·JUAREZ HENEQUEN·Product code BTO·August 16, 2007
DIC LARYNGECTOMY; DIC TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·NULL·Product code BTO·September 24, 2022
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·February 24, 2014
CONTACT DETACH
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 10, 2025
TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 1, 2010
TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·September 1, 2010
TALENT THORACIC STENT GRAFT SYSTEM - COILTRAC
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·September 1, 2010
SHILEY DESPOSABLE INNER CANNULA
FDA Adverse Event
Malfunction
·MALLINCKRODT, INC.·Product code BTO·May 21, 2001