28 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

RAICHEM CALCIUM (OCPC) LIQUID REAGENT

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Humeral Cup Stability

FDA UDI
FX SOLUTIONS·03701037308066·STABILITY TRIAL CUP Ø40 +9

POSTERIOR DISTAL TIBIA PLATE , LEFT

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665024876·

Humeral Cup Stability

FDA UDI
FX SOLUTIONS·03701037309469·HUMERAL CUP STABILITY PE/TA6V Ø40/+9

LEONE SPA

FDA UDI
LEONE SPA·08033707002086·CHROMIUM-COBALT WIRE 0,9mm

RANDOX C-REACTIVE PROTEIN

FDA 510(k)
FDA Class 2 ·Immunology

WHITE MTA MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

9616026-2006-00240

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

9616026-2006-00244

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00239

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00222

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

9616026-2006-00252

FDA Adverse Event
Other ·Product code FII·June 21, 2006

9616026-2006-00245

FDA Adverse Event
Malfunction ·Product code FII·June 22, 2006

9616026-2006-00253

FDA Adverse Event
Other ·Product code FII·June 21, 2006

PRISMAFLEX SYSTEM

FDA Adverse Event
Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code MQS·June 8, 2006

9616026-2006-00221

FDA Adverse Event
Malfunction ·Product code FII·June 21, 2006

PRISMAFLEX SETS (M)

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·May 13, 2024