40 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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CLEVER CHEK TD-3250C BLOOD GLUCOSE PLUS BLOOD PRESSURE MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
INTERSURGICAL INTERFORM INTUBATING STYLET, SIZE 14FR, OD 4.7MM
FDA UDI
Intersurgical Incorporated·05030267109579·INTERSURGICAL INTERFORM INTUBATING STYLET, SIZ...
Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613215135·STRYKER® OSCILLATING BLADE REPLACEMENT
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014604015·MIDMARK DELUXE-7100 2"POLYFOAM W/SOFTCARE CVR
ConMed Linvatec
FDA UDI
Provision·B504OM50800140·
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037309124·SLEEVE Ø14mm
VADER Pedicle System, Rod, Ti, straight, Ø 6.0 r000 x 140 mm
FDA UDI
icotec AG·07640164847184·VADER Pedicle System, Rod, Ti, straight, Ø 6.0 ...
BARCOMED 5MP1H
FDA 510(k)
FDA Class 2
·Radiology
INSTANT-VIEW METHADONE URINE DIP STRIP TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR AND GENFIND DNA EXTRACTION KIT
ASSURE WEARABLE CARDIOVERTER DEFIBRILLATOR
FDA Adverse Event
Malfunction
·KESTRA MEDICAL TECHNOLOGIES, INC.·Product code MVK·November 19, 2025
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HUMAN PAPILLOMA VIRUS (HPV) HIGH RISK (HR)
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR TEST
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HUMAN PAPILLOMA VIRUS (HPV)
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR ASSAY
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·Cervista® HPV HR Assay
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR, GENFIND DNA EXTRACTION KIT
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·CERVISTA HPV HR
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·Cervista HPV HR Assay