40 results · 19ms · Sources: EU EUDAMED, 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