10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
SEIRIN JR ACUPUNCTURE NEEDLES
FDA 510(k)
FDA Class 2
·General Hospital
artegral
FDA UDI
Merz Dental GmbH·D7091970260·anteriors; shade B4; mould UIS
BC-001+ Acne Purifier
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
STAR ST AND ARRHYTHMIA SOFTWARE, RELEASE H.0
FDA 510(k)
FDA Class 2
·Cardiovascular
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code CBK·June 29, 2017
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 29, 2014
ADAPTER SLEEVE 11/13 +0
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 20, 2013
LUMBAR SCREW 6,7 X 40 MM + BALL RING
FDA Adverse Event
Injury
·STRYKER SPINE BORDEAUX·Product code MNH·January 14, 2011
Urine Reagent Strips (URS) 11 Parameters URS-11-100G-001 510(K) number: K970250 Devise Listing number: D072377 Each Device consists of 100 strips of Urine Reagent Strips 11 parameters packed with a desiccant pouch inside a black bottle with Cortez Diagnostics Label on the bottle and the bottle placed inside a Cortez Diagnostics Box.
FDA Recall
Terminated
·Teco Diagnostics·Product code KQO·October 14, 2011
Urine Reagent Strips (URS) 10 Parameters URS-l0-100W 510(K) number: K970250 Devise Listing number: D072377 Each device consists of 100 strips of Urine Reagent Strips 10 parameters packed with a desiccant pouch inside a gray bottle with Teco Diagnostics Label on the bottle and the bottle placed inside a Teco Diagnostics Box. For the semi-quantitative and qualitative detection of Glucose, Bilirubin, Ketone, Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite, Leukocytes in urine.
FDA Recall
Terminated
·Teco Diagnostics·Product code KQO·October 14, 2011