SEARCH RESULTS FOR: 出海电商0成本推广🚩TG@yuantou2048🚩最快24小时见效出海推广营销一条龙(6856 results)
Battery and Electrode Cartridge
HEARTSINE TECHNOLOGIES LTD
Pad-Pak-01
PAD-PAK-01
- Non-rechargeable public semi-automated external defibrillation electrode, adult
Replacement MOU for the EXOGEN® Ultrasound Bone Healing System, device identifier M937710346001.
BIOVENTUS LLC
71034601
In Commercial Distribution
- M937710346011 ()
71034601
- Bone growth ultrasonic stimulator
The EXOGEN device provides non-invasive therapy for healing non-unions and accelerating time to healing of fresh fractures. The EXOGEN Ultrasound Bone Healing Systems has been designed both for use with conservatively treated fresh fractures and non-unions or surgically treated non-unions. The device transmits a low intensity ultrasound signal to the fracture site through coupling gel, with little or no sensation felt by the patient during the treatment. The low-intensity pulsed ultrasound has been shown in in-vitro and in-vivo studies to stimulate cells to produce growth factors and proteins that are important to bone healing. The patient administers treatment at home or at work, once daily, for 20 minutes, or as prescribed by a physician. The device automatically alerts the patient in case of improper application or device performance. The EXOGEN Ultrasound Bone Healing System consists of one main operating unit, gel bottles and strap. The main operating unit provides the treatment control circuitry, the primary battery supply, and monitors the operation of the transducer at the fracture site. The signal specifications cannot be changed.
BIOVENTUS LLC
71034600
In Commercial Distribution
- M937710346001 ()
71034600
- Bone growth ultrasonic stimulator
- Radiographic image marker, manual
- Skin topical coupling gel
- Personal device holder, single-use
The EXOGEN Ultrasound Bone Healing System provides non-invasive therapy for healing non-unions and accelerating time to healing of fresh fractures. EXOGEN is designed both for use with conservatively treated fresh fractures and non-unions, or surgically-treated non-unions. EXOGEN transmits a low-intensity ultrasound signal to the fracture site through coupling gel, with little or no sensation felt by the patient during the treatment. Low-intensity pulsed
ultrasound has been shown in in-vitro and in-vivo studies to stimulate cells to produce growth factors and proteins that are important to bone healing.
The patient administers treatment at home or at work, once daily, for 20 minutes, or as prescribed by a physician. EXOGEN automatically alerts the patient in case of improper application or performance. The EXOGEN Ultrasound Bone Healing System consists of one EXOGEN device, a charger, a gel bottle and strap. The EXOGEN device provides the treatment control circuitry, the battery supply and monitors the operation of the transducer at the fracture site. Thesignal specifications cannot be changed.
BIOVENTUS LLC
71034400
In Commercial Distribution
- M937710344001 ()
71034400
- Bone growth ultrasonic stimulator
- Radiographic image marker, manual
- Skin topical coupling gel
- Personal device holder, single-use
- Noninvasive device battery charger
Powerheart® G3 Elite AED, Fully Automatic, Korea (No battery or pads)
Zoll Medical Corporation
9790A-19
In Commercial Distribution
- 00812394023158 ()
9790A-19
- Non-rechargeable public automated external defibrillator
Powerheart® G3 Elite AED, Fully Automatic, Korean, with Adult Pads and Battery
Zoll Medical Corporation
9790A-1019
In Commercial Distribution
- 00812394023110 ()
9790A-1019
- Non-rechargeable public automated external defibrillator
Powerheart® G3 Elite AED, Semi Automatic, Korea (No battery or pads)
Zoll Medical Corporation
9790E-10
In Commercial Distribution
- 00812394023165 ()
9790E-19
- Non-rechargeable public semi-automated external defibrillator
Powerheart® G3 Elite AED, Semi-Automatic, Korean, with Adult Pads and Battery
Zoll Medical Corporation
9790E-1019
In Commercial Distribution
- 00812394023127 ()
9790E-1019
- Non-rechargeable public semi-automated external defibrillator
MINERVA RF Controller
Contents:
(1) One MINERVA RF-Controller
(1) One Footswitch
(1) One Power Cord
Minerva Surgical, Inc.
MIN180S
In Commercial Distribution
- 00862393000100 ()
MIN180S
- Inert gas-enhanced endoscopic electrosurgical submucosal lift/resection instrument
The intended use for the ML6710i laser is photoactivation of VISUDYNE® (verteporfin for injection), which is a light-activated drug used in photodynamic therapy (PDT) for the treatment of patients with predominantly classic subfoveal choroidal neovascularization due to age-related macular degeneration, pathologic myopia or presumed ocular histoplasmosis.
Please consult the VISUDYNE® (Bausch & Lomb Incorporated) prescribing information for additional information on intended use, recommended drug and light dose, administration instructions, contraindications, warnings and precautions, and side effects of VISUDYNE® treatment.
Modulight Oyj
ML6710i
In Commercial Distribution
- 06429810677020 ()
- Ophthalmic diode laser system