26 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Maxpower Relief
FDA 510(k)
FDA Class 2
·Neurology
Impact™
FDA UDI
B BRAUN INTERVENTIONAL SYSTEMS, INC·04046964291173·IMPACT BALLOON CATHETER 18MMX2CMX120CM
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269408·
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704513110·
Percutaneous Compression Plate (PC.C.P)
FDA UDI
ORTHOFIX SRL·18032568866063·GOTFRIED PC.C.P. NECK SCREW - 120 MM
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM46001822061201·Rotary instrument for endodontic application
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100974·DESMARRES LID RETRACTOR #2
Percutaneous Compression Plate (PC.C.P)
FDA UDI
ORTHOFIX SRL·18033509850561·GOTFRIED PC.C.P. NECK SCREW - 120 MM STERILE
KING Snap Lead/DIN Connector
FDA UDI
Kego Corporation·00663427000109·KING Snap Lead/DIN Connector Qty 5
3.0 m (120")...
S-Type QR Fitting: Helios
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215039585·
NIPPV SILICONE FACE MASK, NIPPV ECONOMY FACE MASK, NIPPV SILICONE NASAL MASK MODEL 10212, 10222, 10202
FDA 510(k)
FDA Class 2
·Anesthesiology
AEQUALIS REVERSED FRACTURE SHOULDER PROTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
MOTO PARTIAL KNEE TIBIAL TRAY FIX CEMENTED S1 RM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·May 31, 2022
1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024
ARMADA 14 PTA CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LIT·June 21, 2013
VM1
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 4, 2014
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 23, 2011
PEN NDL 32G 4MM PRO 100 BOX 1200 US
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021
BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023