44 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Signia Small Diameter Reloads
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112328·SURG-I-BAND GREEN
THINFLAP SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036088491·
Sklar®
FDA UDI
SKLAR CORPORATION·10649111117329·DRESSING FORCEP SERR 7"
Trocar sleeve
FDA UDI
SOPRO-COMEG GmbH·04059082005089·
EXPEDIUM SPINE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MANOSCAN MOTILITY WITH IMPEDANCE VISUALIZATION SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918147604·Waste Containment Bowl_Yellow_assembled_non-ste...
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918137414·Waste Containment Bowl_Red_assembled_non-steril...
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918147390·Waste Containment Bowl_Red_sterile_20ea/cs
Alleset
FDA UDI
GRI Medical & Electronic Technology Co., Ltd.·16931918144849·Waste Containment Bowl_Yellow_sterile_20ea/cs
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 21, 2014
PINNACLE MTL INS NEUT36IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·June 26, 2013
SECNDRY SET 34IN NDEHP
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code FPK·July 25, 2011
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 2, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·June 2, 2022
SUPERSHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO. LTD.·Product code DRE·August 12, 2018
SUPERSHEATH
FDA Adverse Event
Malfunction
·TOGO MEDIKIT CO. LTD.·Product code DRE·December 11, 2016
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO.LTD.·Product code DRE·January 18, 2018
SUPER SHEATH
FDA Adverse Event
Injury
·TOGO MEDIKIT CO., LTD.·Product code DRE·March 21, 2023