24 results
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47ms
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Sources: EU EUDAMED, US FDA
FlexTEMP System, Sensor - 989803178171
FDA registration
Philips North America LLC·1 product·🇺🇸 United States
Amphenol Medical Technologies (Dongguan) Co., Ltd.
FDA registration
Amphenol Medical Technologies (Dongguan) Co., Ltd.·1 product·🇨🇳 China
Expression MR400 MRI Patient Monitoring System
FDA registration
DHL SUPPLY CHAIN (NETHERLANDS) B.V.·1 product·🇳🇱 Netherlands
FlexTEMP System, Sensor - 989803178171
FDA registration
Philips Electronics Ltd·1 product·🇨🇦 Canada
FlexTEMP System, Sensor - 989803178171
FDA registration
INVIVO CORPORATION·1 product·🇺🇸 United States
FlexTEMP System, Sensor - 989803178171
FDA registration
Philips North America LLC·1 product·🇺🇸 United States
Expression MR400 MRI Patient Monitoring System
FDA registration
Sanmina-SCI Systems Singapore Pte. Ltd.·1 product·🇸🇬 Singapore
INVIVO CORPORATION
FDA registration
FABRINET CO., LTD.·1 product·🇹🇭 Thailand
CBR ENTERPRISE LIMITED
FDA registration
CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong
Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.
FDA registration
Amphenol Cable and Interconnect Technologies Asia Pacific Ltd.·1 product·🇭🇰 Hong Kong
Expression MR400 MRI Patient Monitoring System
FDA 510(k)
FDA Class 2
·Cardiovascular
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100301·INFANT WIRE SPECULUM 3MM/5MM BLADES
Ophthalmic Forceps
FDA UDI
KATENA PRODUCTS, INC.·00841668106273·KELMAN-MCPHERSON FORCEPS 1X2 TEETH
AMSCO V-PRO maX Low Temperature Sterilization System (MY-CFE)
FDA registration
STERIS MEXICO, S. de R.L. de C.V.·1 product·🇲🇽 Mexico
AMSCO V-PRO maX Low Temperature Sterilization System (MY-CFE)
FDA registration
STERIS Corporation·1 product·🇺🇸 United States
AMSCO V-PRO maX Low Temperature Sterilization System (MY-CFE)
FDA registration
STERIS CORPORATION·1 product·🇺🇸 United States
KOWA VX-20
FDA registration
KOWA CO. LTD. CHOFU·2 products·🇯🇵 Japan
HeartLight Deflectable Sheath
FDA registration
STERILIZATION SERVICES OF VIRGINIA·2 products·🇺🇸 United States
PF 6001 Main Unit
FDA registration
PERIMED AB·1 product·🇸🇪 Sweden
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)