31 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex Univers Apex, Size 5 Stem
FDA 510(k)
FDA Class 2
·Orthopedic
Poly Per-Q-Cath Catheter
FDA UDI
Bard Access Systems, Inc.·00801741034824·Poly Per-Q-Cath Catheter 3F Single-Lumen Basic ...
Poly Per-Q-Cath Catheter
FDA UDI
Bard Access Systems, Inc.·00801741035470·Poly Per-Q-Cath Catheter with Sherlock Tip Loca...
Unicondylar Interpositional Spacer
FDA UDI
Zimmer, Inc.·00889024487024·
Unicondylar Interpositional Spacer
FDA UDI
Zimmer, Inc.·00889024487031·
Large CTRPulse Knee Retractor
FDA UDI
Zimmer, Inc.·00889024584129·
Small CTRPulse Knee Retractor
FDA UDI
Zimmer, Inc.·00889024584136·
XIA SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
PRODIGY DIABETES MANAGEMENT SOFTWARE
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ADAPTER NUT
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·March 15, 2011
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·May 19, 2026
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·September 24, 2025
ACQUIRE? PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 10, 2025
EXPECT PULMONARY
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·November 14, 2024
EXPECT PULMONARY
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FCG·April 14, 2026
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 8, 2013
DUAL COOLER/HEATER
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·June 17, 2011
VAPR SE ELECTRODE
FDA Adverse Event
Injury
·DEPUY MITEK·Product code GEI·September 8, 2008
UNK - ELASTIC NAILS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code JDS·December 7, 2020
UNK - ELASTIC NAILS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code JDS·December 7, 2020