Medical device - Import export

MUSTANOGLU PROFESSIONAL MEDICAL EQUIPMENTS SALON DEVICESREGIONAL REVIEW REGIONAL THINNING DIODE LASER EMS SLIM EMS HIEMT 7D HIFU 4D HIFU HYDRAPRO Q-SWITCH PLASMA G5 LENF DRAINAGE INBODY PDT SKIN ANALYSIS ROLL SLIM

•21 gauge lancet 2.0mm •Suggested test areas e.g. cholesterol, Haemoglobin (Hgb), diagnostic kit tests such as cardiac enzymes Side fire activation Unistik 3 puts the sampling experience firmly in your hands, with side-fire activation enabling you to decide exactly when to activate the device and how much pressure to apply. The alignment guide indicates precisely where the device will activate on the patient’s finger.

Disinfectant solution for medical devices

The work of the TempoHeart module is based on the method of scoring the heart rate vegetative regulation. This method is popular due to its high information value and non-invasiveness. Cannot be used without an interface block. The module can: • evaluate the heart rate autonomic regulation; • to predict in advance (to prematurely reveal) the hazards of a myocardial infarction, hypertensive crises and strokes; • to determine the metabolic and electrolyte disorders in the myocardium; • identify risk groups for heart rate increased stability; • to make a cold evaluation of the autonomic nervous system's reaction when exposed to electromagnetic fields, intoxications and other pathogenic factors; • to assess the activity of the respiratory component when measuring heart rate variability, recording the parameters of blood movement in the vessels; • to expose the stress resistance level.

Features a circumferential, semi-rigid shell that offers maximum support to the leg/ankle following injury or post-operative procedures. Available in a high boot (pictured) and low boot version. Product Features: Streamlined, semi-rigid shell is lightweight yet provides maximum support for the leg and ankle. Medial/lateral air bladders offer customized compression to increase comfort and reduce edema. Rocker sole helps promote a natural gait to allow continuation of daily activities. Shock-absorbing insole reduces impact of the heel strike while walking. Toe guard for added protection.

We are able to supple all kind of medical products, however our main products lines are diabetic cares, dermal filler and laboratory reagents.

HYAcorp Body Contouring MLF2© is an absorbable skin implant with a high level of purity. It is a medical device intended for single use only and is produced from a hyaluronic acid of non-animal origin. The special composition of HYAcorp Body Contouring MLF2© provides maximal volumizing results in body contouring.

ALIAXIN® GP (Global Performance) is a resorbable medical device to be used as a filler for the correction of medium and deep facial cutaneous sagging and to increase the volume and contours of the lips. The principal component is cross-linked Hyaluronic Acid of non-animal origin, produced by bacterial fermentation.

HYAcorp FINE© is an absorbable skin implant with a high level of purity. It is a medical device intended for single use only and is produced from a hyaluronic acid of non-animal origin. HYAcorp FINE© contains natural HA to moisturize the skin.

HYAcorp Body Contouring MLF1© for body contouring is a resorbable high-purity skin implant-filler, which contains a pure viscous gel from cross-linked hyaluronic acid. That is a medical device for single use, designed specifically for giving the body contours, forming zones of buttocks, calves and correcting defects in the form of depressions.

Syringe Testing is a critical step in developing and commercializing needlebased injection systems for medical use. By testing mechanical properties, such as breakloose and glide force, as well as biocompatibility, extractables and leachables, sterility, packaging and transit properties, we can determine if the device is within standard specifications, reducing the likelihood of improper function. Eurofins Medical Device Testing network of laboratories has experience performing an array of standard and nonstandard testing on syringes to verify their safety. Choose Eurofins Medical Device Testing to help you Determine the necessary testing requirements for your device Write GMPcompliant and ISO standard driven protocols and methods Perform the required tests to demonstrate that the expected performance criteria are satisfied Complete batch release activities and/or gain regulatory approval

Simplify product discovery with the largest EU CTD dossier database. Expert curated, up-to-date information. Powerful search engine and product filters. Product categories include: generics, biosimilars, medical devices & nutraceuricals for human use. GMP approved factories. All therapy areas.

Class I of Regulation EU 2017/745 on medical devices; Type II R (liquidresistant), tested according to EN 14683 2019 for surgical masks. The inside and outside are made of physiologically harmless, plasticizerfree polypropylene fleece, the filter medium consists of a special microfiber fleece produced using the meltblown process, welded together using the ultrasound process.

Class I of Regulation EU 2017/745 on medical devices; Type II R (liquidresistant), tested according to EN 14683 2019 for surgical masks. The inside and outside are made of physiologically harmless, plasticizerfree polypropylene fleece, the filter medium consists of a special microfiber fleece produced using the meltblown process, welded together using the ultrasound process.

Class I of Regulation EU 2017/745 on medical devices; Type II R (liquidresistant), tested according to EN 14683 2019 for surgical masks. The inside and outside are made of physiologically harmless, plasticizerfree polypropylene fleece, the filter medium consists of a special microfiber fleece produced using the meltblown process, welded together using the ultrasound process.

Class I of Regulation EU 2017/745 on medical devices; Type II R (liquidresistant), tested according to EN 14683 2019 for surgical masks. The inside and outside are made of physiologically harmless, plasticizerfree polypropylene fleece, the filter medium consists of a special microfiber fleece produced using the meltblown process, welded together using the ultrasound process.

Class I of Regulation EU 2017/745 on medical devices; Type II R (liquidresistant), tested according to EN 14683 2019 for surgical masks. The inside and outside are made of physiologically harmless, plasticizerfree polypropylene fleece, the filter medium consists of a special microfiber fleece produced using the meltblown process, welded together using the ultrasound process.

Disinfectant solution for medical devices

Concentrated disinfectant solution for medical devices

Concentrated disinfectant solution for Medical Devices

Disinfectant solution for medical devices 2 % Glutaraldehyde

Concentrated disinfectant solution for medical devices Peracetic Acid 3840 %

Disinfectant solution for medical devices Peracetic Acid 1,2 %

Concentrated disinfectant solution for medical devices 2 % Gluteraldehyde

A&D and Omron Blood Pressure Monitors, Digital Thermometers, Nebulisers, Wheeze Detector and Oximeter

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