20 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Reprocessed Steerable/Guiding Sheath
FDA registration
INNOVATIVE HEALTH, LLC.·1 product·🇺🇸 United States
Reprocessed VersaCross Steerable Sheath; Reprocessed SureFlex Steerable Guiding Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
Reprocessed Catheter Introducer
FDA classification
FDA Class 2
·Reprocessed Catheter Introducer
RIGIDLOOP
FDA UDI
Medos International Sàrl·10886705022830·RIGIDLOOP Disposables Kit 4.5mm Cannulated Ream...
CD Horizon Spinous Plate
FDA registration
WARSAW ORTHOPEDIC, INC.·4 products·🇺🇸 United States
CD Horizon Spinous Plate
FDA registration
Medtronic Medical Costa Rica S.R.L.·4 products·🇨🇷 Costa Rica
CD Horizon Spinous Plate
FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·4 products·🇺🇸 United States
Accutorr 3,VS-600 Vital Signs Monitor
FDA registration
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.·4 products·🇨🇳 China
CD HORIZON (ADDITION OF SPINOUS PROCESS PLATE)
FDA registration
UNITED ORTHOPEDIC CORP.·4 products·🇹🇼 Taiwan
CD Horizon Spinous Plate
FDA registration
Medtronic Engineering and Innovation Center (MEIC)·4 products·🇮🇳 India
Accutorr 3,VS-600 Vital Signs Monitor
FDA registration
Shenzhen Mindray Bio-Medical Electronics Co.,LTD·4 products·🇨🇳 China
CD Horizon Spinous Plate
FDA registration
MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·4 products·🇺🇸 United States
Atalante X
FDA registration
Wandercraft Incorporated·1 product·🇺🇸 United States
BUHLMANN fCAL® turbo (fecal calprotectin turbidimetric assay), CALEX® Cap (stool preparation device)
FDA registration
BUHLMANN LABORATORIES AG·1 product·🇨🇭 Switzerland
Atalante X
FDA registration
WANDERCRAFT·1 product·🇫🇷 France
CAPI 3 NEONAT HB USING THE CAPILLARYS 3 DBS INSTRUMENT
FDA registration
SEBIA·1 product·🇫🇷 France
CD HORIZON (ADDITION OF SPINOUS PROCESS PLATE)
FDA 510(k)
FDA Class 2
·Orthopedic
VITAL SIGNS MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Orthosis, Spinal Pedicle Fixation
FDA classification
FDA Class 2
·Orthosis, Spinal Pedicle Fixation