3,273 results
·
20ms
·
Sources: EU EUDAMED, US FDA
LX9max
FDA UDI
DAESUNG MAREF CO.,LTD.·08809315675222·Main device 1ea, LEG SLEEVE XXLarge 2ea, ARM SL...
COR18000148-000
FDA Adverse Event
No answer provided
·Product code RFZ·February 12, 2018
COR22000011-000
FDA Adverse Event
No answer provided
·Product code RFZ·January 25, 2022
Motorola Solutions PCS3000/CS3070 Laser Utility/Peripheral Laser Products
FDA Recall
Terminated
·Motorola Inc·Product code RFZ·April 27, 2012
Hemochron Signature Elite Whole Blood Microcoagulation (IVD) System. The system is intended to be used only with test cuvettes that are available from ITC.
FDA Recall
Terminated
·International Technidyne Corp.·Product code RFZ·March 31, 2010
Upc Scanner Reader (Bar Code Reader)
FDA classification
FDA Not Classified
·Upc Scanner Reader (Bar Code Reader)
RFB Latex Limited
Manufacturer
🇮🇳 India·1 Basic UDI-DI·1 Device
Raz Design Inc.
Manufacturer
🇨🇦 Canada·3 Importers
RFH - Rehatechnik GmbH
Manufacturer
🇩🇪 Germany
RFB Gloves
FDA registration
RFB Gloves·2 products·🇮🇳 India
RFI Hygiene Limited
FDA registration
RFI Hygiene Limited·7 products·🇨🇳 China
RAZ DESIGN INC.
FDA registration
RAZ DESIGN INC.·1 product·🇨🇦 Canada
Multigate Co., Ltd
Manufacturer
🇨🇳 China·48 Basic UDI-DIs·331 Devices
RFX+CARE Manufacturing Co., Ltd.
Manufacturer
🇨🇳 China·104 Basic UDI-DIs·315 Devices·5 Importers·TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, TÜV SÜD Product Service GmbH, and TÜV SÜD Product Service GmbH
RFA PAKKET
Device
EU MDR
·
Eu Md Class 2a
·On the market
Penguin RFA
Device
EU MDR
·
Eu Md Class 1
·Integration Diagnostics / NSK Nordic·On the market·1 country
RFA PAKKET
Device
EU MDR
·
Eu Md Class 2a
·On the market
RFA PAKKET
Device
EU MDR
·
Eu Md Class 2a
·On the market
NEGATIVE MIC 38
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JWY·November 14, 2014
PFZ PORCELAIN SYSTEM
FDA 510(k)
FDA Class 2
·Dental