24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RENASYS TOUCH Negative Pressure Wound Therapy, RENASYS TOUCH Canisters, RENASYS TOUCH Carry Bag, Carry Strap, RENASYS Y-Connector, RENASYS TOUCH IV Pole/Bed Clamp, RENASYS TOUCH Class 2 Power Supply
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Oticon
FDA UDI
Oticon A/S·05707131292131·ALTA2 PRO, BTE 13 WL 105 SIL
Symmetry Hartman
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482035689·Symmetry® Forceps, Hartman Baby Mosquito, Strai...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364473·Medullary canal orthopaedic reamer, rigid - End...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364466·Medullary canal orthopaedic reamer, rigid - End...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364459·Medullary canal orthopaedic reamer, rigid - End...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575364442·Medullary canal orthopaedic reamer, rigid - End...
TANGO+ AUTOMATIC BLOOD PRESSURE AND OXYGEN SATURATION MEASUREMENT SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
VERIGENE RESPIRATORY VIRUS NUCLEIC ACID TEST +(RVNAT+)
FDA 510(k)
FDA Class 2
·Microbiology
HNM Medical
FDA UDI
HNM STAINLESS, LLC.·00842962111284·BABY HARTMAN MOSQUITO FORCEPS, 3 7/8", STR
BAXJECT II HI-FLOW
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026
BAXJECT II HI-FLOW
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026
BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026
BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026
BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 26, 2024
ELECTRODE, PACEMAKER, PERMANENT
FDA Adverse Event
Injury
·MPRI·Product code DTB·June 8, 2013
COGNIS
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 7, 2011
RENEGADE? HI-FLO? KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - CORK·Product code KRA·October 8, 2014
BD VACUTAINER® ULTRATOUCH¿ PUSH BUTTON BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·April 15, 2024
BAXJECT II HI-FLOW
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A INC.·Product code LHI·May 4, 2026