9,652 results
·
51ms
·
Sources: EU EUDAMED, US FDA
FERTILE ULTIMATE
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·KOEK BİYOTEKNOLOJİ BİYOMÜHENDİSLİK VE MEDİKAL HİZ. SAN. TİC. A.Ş.·1 device
FERTILE PLUS
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·KOEK BİYOTEKNOLOJİ BİYOMÜHENDİSLİK VE MEDİKAL HİZ. SAN. TİC. A.Ş.·1 device
Fertile
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·KOEK BİYOTEKNOLOJİ BİYOMÜHENDİSLİK VE MEDİKAL HİZ. SAN. TİC. A.Ş.·1 device
ZyMōt™ Multi (3ml)
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·KOEK BİYOTEKNOLOJİ BİYOMÜHENDİSLİK VE MEDİKAL HİZ. SAN. TİC. A.Ş.·1 device
ZyMōt™ Multi (850µl)
Basic UDI-DI
EU MDD
·
Eu Md Class 2a
·KOEK BİYOTEKNOLOJİ BİYOMÜHENDİSLİK VE MEDİKAL HİZ. SAN. TİC. A.Ş.·1 device
Cochlear Implant With Combined Electrical Stimulation And Acoustic Amplification
FDA Pre-Market Approval
FDA Class 3
·NUCLEUS HYBRID L24 COCHLEAR IMPLANT SYSTEM
TNP/MDR/0018/3830/2024
Certificate
MDR QMS·FOLDIX MEDICAL INŻ. UWE WERNER PETRASCH·TUV NORD Polska Sp. z o.o
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WAVELIGHT ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·ALLEGRETTO WAVE EYE-Q LASER SYSTEM
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·APTIMA HPV ASSAY
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·WAVELIGHT ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM
Knife, Ophthalmic, Reprocessed
FDA classification
FDA Class 1
·Knife, Ophthalmic, Reprocessed
Atomic Absorption, Arsenic
FDA classification
FDA Class 1
·Atomic Absorption, Arsenic
Telescope, Laryngeal-Bronchial
FDA classification
FDA Class 2
·Telescope, Laryngeal-Bronchial
Imager, Breast, Electrical Impedance
FDA Pre-Market Approval
FDA Class 3
·TS2000
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·COMBI 40+ COCHLEAR IMPLANT SYSTEM
Blade, Keratome, Reprocessed
FDA classification
FDA Class 1
·Blade, Keratome, Reprocessed
Sets de soins cutanés et de plaies
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·88 devices
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·COMBI 40+COCHLEAR IMPLANT SYSTEM