19 results
·
19ms
·
Sources: EU EUDAMED, US FDA
STANFORD STERILE LAP SPONGES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Cavitron®
FDA UDI
Dentsply Professional·D00388001021·Cavitron® integrated systems Built-In Ultrasoni...
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950022595·WIRE TUBE 24G (50) 18" STRANDS PER TUBE NS
BaseVac
FDA UDI
R. E. Morrison Equipment Inc·D13028001020·4 User Single Pump System | 1.2 Hp w/ Exhaust Kit
THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope
FDA UDI
THD SPA·08033737710470·THD Light-Scope anoscope is a disposable medica...
MyndStep
FDA UDI
MyndTec Inc·00692520001027·MyndStep is a wearable foot drop device, which ...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690123767·Headed Steinman Pin 1.39"
0800,APS1,08,N,LT,VL
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828152839·0800,APS1,08,N,LT,VL
ADP,1,P800,S800,(2)1/4",N,TV,JERON
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828118422·ADP,1,P800,S800,(2)1/4",N,TV,JERON
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756015776·ARM SLING
GLUCOSE (HEXOKINASE) LIQUID REAGENT, MODEL G518-150
FDA 510(k)
FDA Class 2
·Clinical Chemistry
TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197077811·Horizontal Bar
438mm,...
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 8, 2014
ACCU-CHEK SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·October 17, 2012
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS INC.·Product code LYJ·August 11, 2010
OLYMPUS
FDA Adverse Event
Other
·OLYMPUS OPTICAL CO., LTD.·Product code EOQ·June 5, 1998
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 23, 2017
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 23, 2017