887 results · 39ms · Sources: EU EUDAMED, US FDA

JEDMED

FDA UDI
JEDMED INSTRUMENT COMPANY·M633036151L0·Classic CSC-SDL Cabinet SC/PRS 240V

SMR MAXI CABINET, STAINLESS STEEL, STANDARD, NO OTOSCOPES

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252303·

SMR MAXI CABINET, STAINLESS STEEL, DELUXE, CORDED OTOSCOPES, 220-240V, REQUIRES

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252402·

SMR MAXI CABINET, STAINLESS STEEL, DELUXE-TALL, RECHARGEABLE OTOSCOPES

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252457·

MTI

FDA UDI
Medical Technology Industries, Inc.·10840118439968·TC100AS ENT Cabinet, Sit-down, Std Config 1 LAM...

TALL TREATMENT CABINET, LAMINATE, CORDED OTOSCOPES, DIAGNOSTIC

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252822·

OTOPRONT

FDA UDI
Happersberger Otopront GmbH·04260154541002·

JEDMED

FDA UDI
JEDMED INSTRUMENT COMPANY·M6330360050·SINUPRO CART COMPLETE

SMR MAXI CABINET, ALUMINUM COMPOSITE, STANDARD-TALL, NO OTOSCOPES, 220-240V, REQ

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252631·

SMR MAXI CABINET, ALUMINUM COMPOSITE, STANDARD-TALL, RECHARGEABLE OTOSCOPES

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040252600·

DISPOSABLE HYDROPHOBIC HEPA FILTER FOR CABINET SUCTION LINE - 24 PACK

FDA UDI
GLOBAL SURGICAL CORPORATION·00810040253195·

Stimulator, Electrical, Implantable, For Incontinence

FDA Pre-Market Approval
FDA Class 3 ·MEDTRONIC INTERSTIM THERAPY

AIXPLORER

FDA 510(k)
FDA Class 2 ·Radiology

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·ADVISA DR IPG, ADVISA DR MRI IPG

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MARQUIS DR ICD, MARQUIS VR ICD, MAXIMO DR ICD AND MAXIMO VR ICD

FDA Pre-Market Approval
INSYNCC III MARQUIS ICD, INSYNC MAXIMO ICD

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·REVO MRI IPG

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval
FDA Class 3 ·CONSULTA CRT-P, SYNCRA CRT-P

Aura Wellness

FDA UDI
Aura Wellness, LLC·00850026680010·The Butterfly Loop PEMF accessory coil is used ...

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·RES-Q(TM) ARRHYTHMIA CONTROL DEVICE SYSTEMS