306 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Etest Ceftazidime/Avibactam (CZA) (0.016 - 256 ug/mL)
FDA 510(k)
FDA Class 2
·Microbiology
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780360988·Integra® Miltex® Microsurgery Scissors 5-3/4", ...
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100769·FLIERINGA FIXATION RING 15MM
Symmetry Schnidt
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482056868·Symmetry® Forceps, Schnidt Artery, 1 Open Ring,...
Ophthalmic Ring
FDA UDI
KATENA PRODUCTS, INC.·00841668100820·FLIERINGA FIXATION RING 21MM
DIMER ACID DERIVED NANO-HYBRID COMPOSITE RESTORATIVE MATERIAL
FDA 510(k)
FDA Class 2
·Dental
SYNGO DYNAMICS, VERSION 9.0
FDA 510(k)
FDA Class 2
·Radiology
HNM Medical
FDA UDI
HNM STAINLESS, LLC.·00842962112052·SCHNIDT ARTERY FORCEPS, 7 1/2", 1 OPEN RING
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 11, 2013
COULTER LH 750 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·June 15, 2011
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 25, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 30, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 5, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·June 29, 2022
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 22, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 30, 2021