16 results
·
21ms
·
Sources: EU EUDAMED, US FDA
RefleXion Medical Radiotherapy System, Reflexion X2
FDA 510(k)
FDA Class 2
·Radiology
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252071200·ceraMotion® Me Incisal Transpa 2, 20 g / dental...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197175135·Antrum Curette oval Fig. 1
7mm, 2...
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252071400·ceraMotion® Me Incisal Transpa 2, 40 g / dental...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197175142·Faulkner Antrum Curettes
220mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197175227·Faulkner Antrum Curettes
220mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197393126·FAULKNER Antrum curette,
220mm,...
LYSUS INFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
NovaBone MacroFORM MIS Composite - 2.5cc, NovaBone MIS Cartridge Delivery System (cartridge handle only)
FDA 510(k)
FDA Class 2
·Orthopedic
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·November 14, 2014
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 16, 2011
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 29, 2013
CEFALY
FDA Adverse Event
Injury
·CEFALY TECHNOLOGY·Product code PCC·March 9, 2026
CEFALY
FDA Adverse Event
Injury
·CEFALY TECHNOLOGY·Product code PCC·March 9, 2026
ION Reprocessing Accessories Kit, IF1000 (Part Number: 490024-03) UDI:00886874119129. The kit includes an ION Catheter Reprocessing Cover (Part Number: 490114-02).
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code EOQ·June 10, 2020
Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
FDA Recall
Open, Classified
·Intuitive Surgical, Inc.·Product code EOQ·June 10, 2020