363 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CARESCAPE Respiratory MOdules, E-sCO, E-sCOV, E-sCOVX, E-sCAiO, E-sCAiOV, E-sCAiOVX and accessories
FDA 510(k)
FDA Class 2
·Anesthesiology
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16721710280·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1672171028060·
SCHWERT
FDA UDI
A. Schweickhardt GmbH & Co. KG·E8961710280·Bone spreaders straight 2,8mm
round ...
EUS BALLOON
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VIEWMATE SYSTEM
FDA 510(k)
FDA Class 1
·Physical Medicine
PRADO™ Lumbar Interbody Fusion System
FDA UDI
Pt. Solutions, LLC·G616RTFH171028150·NON-STERILE PRADO™ T HA PEEK IBF, 17MM H X 10MM...
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 14, 2013
RESTORE ADVANCED RECHARGEABLE
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·June 30, 2011
COLLEAGUE VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021