254 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Dissecting Balloon System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROPELLER HEAD SCREW SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304269194·
OsteoMed
FDA UDI
OSTEOMED LLC·00842528127445·2.0 X 24mm Cannulated Headed Screw, T7
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515026049·Kelley Ret, 3 x 3 1/2", standard handle
KING Snap Lead/DIN Connector
FDA UDI
Kego Corporation·00663427000048·KING Snap Lead/DIN Connector Qty 5
.6 m (24")...
mambo™ modular cervical plate system
FDA UDI
Ulrich GmbH & Co. KG·04052536008124·mambo plate S yellow, 4-hole, length 24 mm
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150747·18F x 2.0cm MiniSPC Low Profile Suprapubic Cath...
MiniSPC Button
FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071148126·18F x 2.0cm MiniSPC Low Profile Suprapubic Cath...
Origin DAA Trial Neck HO
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215055790·
Trial Head
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215038373·
TI-MAX X450
FDA 510(k)
FDA Class 1
·Dental
RPM RESPIRATORY GATING SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
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 24, 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·November 7, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 11, 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 24, 2021
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 26, 2021