31 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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OTELO LL
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704282948·LANGENBECK RETRACTOR 3/8"x1 1/2"
Tasso+ Convenience Kit
FDA UDI
Tasso Inc.·00860006434533·Tasso+ allows self-collection of a capillary bl...
ELMED
FDA UDI
ELMED INCORPORATED·00842180168848·4" X 1/2" GREENBERG RETRACTOR BLADE
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575302857·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575293285·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575302765·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575293292·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575293278·Orthopaedic implant aiming/guiding block, reusa...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575293162·Surgical instrument handle, non-torque-limiting...
REMIN PRO
FDA 510(k)
FDA Class 1
·Dental
EYE SEE MULTIPURPOSE, NO-RUB CONTACT LENS SOLUTION
FDA 510(k)
FDA Class 2
·Ophthalmic
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007242·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 4, 2022
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007297·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007266·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007259·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007273·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007280·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013