245 results
·
29ms
·
Sources: EU EUDAMED, US FDA
SOFT BEAT FETAL HEART RATE ELECTRODE MODEL SBT-7000
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Alpha-Tec Systems
FDA UDI
Alpha-TEC Systems, Inc.·00816085023137·Sodium Citrate Solution
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828117456·GEN4 INTERACTIVE
GEN4 Direct Access
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828107730·GEN4 Direct Access
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828114875·GEN4 INTERACTIVE
GEN4 Direct Access
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828105774·GEN4 Direct Access
GEN4 Direct Access
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828107556·GEN4 Direct Access
GEN4 INTERACTIVE
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828116992·GEN4 INTERACTIVE
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450174586·
SYNCHRON CONTROL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
URINE BENZODIAZEPINES (BENZ) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 92A
FDA 510(k)
FDA Class 2
·Clinical Toxicology
S-ROM*SLEEVE PRX ZTT, 18B-LRG
FDA Adverse Event
Injury
·9616671 DEPUY IRELAND·Product code LPH·March 14, 2013
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·March 1, 2011
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·February 21, 2008
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026
BD PHOENIX¿ NMIC/ID-307
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026