About Used Device - Medical Equipment & Machinery Supplier in Estonia

Used Device, located in Estonia, has an active product count of 136. The company lists a variety of medical equipment and machinery, including CT Scanners, MRI Scanners, Ultrasound Systems, and X-ray Parts & Instruments. Their catalogue includes products such as the Siemens SOMATOM Emotion 16 CT Scanner and the GE Innova 3100IQ Cathlab. Many of their products fall under the HS code 9022.12, which includes medical imaging equipment. The materials used in these products include steel, lead-lined composite housing, and electronic components.

The company's product range is diverse, with a focus on medical imaging equipment. They have a range of CT Scanners, including the Siemens Somatom Definition AS 64 and the Toshiba Aquilion Prime 160 Slice CT Scanner. They also list MRI Scanners, such as the Hitachi Aperto Inspire. OPEN MRI, and Ultrasound Systems like the Philips FD 20 10 CATH LAB. The company's products are used in various medical applications, including diagnostics and treatment.

Product Range and Specialties of Used Device

Used Device's product range includes a variety of medical equipment and machinery. Their CT Scanners, for example, are typically classified as high-grade medical imaging equipment, with specifications such as slice count, detector type, and reconstruction software. Buyers of these products usually require certifications such as CE, FDA, or ISO 13485, and may also request documentation such as test reports, user manuals, and maintenance records. The company's MRI Scanners and Ultrasound Systems also have specific requirements, such as magnetic field strength, gradient performance, and probe types.

The materials used in Used Device's products are typically medical-grade, with properties such as biocompatibility, durability, and resistance to corrosion. The company's products may also be subject to regulations such as those related to radiation safety, electromagnetic compatibility, and medical device registration.

Trade and Export Information - Used Device

Exporters of medical equipment and machinery, like Used Device, typically require compliance with regulations such as those related to medical device registration, radiation safety, and electromagnetic compatibility. Buyers of these products usually require certifications such as CE, FDA, or ISO 13485, and may also request documentation such as test reports, user manuals, and maintenance records. The HS code 9022.12, which includes medical imaging equipment, is commonly used for these products. Trade agreements, such as those related to Incoterms, may also apply to these transactions.

The origin country of Estonia has specific regulations and requirements for the export of medical equipment and machinery. Buyers should be aware of these regulations and ensure that the products they purchase comply with them. The company's products may be subject to inspection and testing before export, and may require special packaging and labeling.

Sourcing from Used Device - Buyer Guidance

When sourcing from Used Device, buyers should request specifications, samples, and test reports to ensure that the products meet their requirements. They should also verify the company's certifications, such as CE, FDA, or ISO 13485, and request documentation such as user manuals and maintenance records. Buyers should be aware of the regulations and requirements related to medical device registration, radiation safety, and electromagnetic compatibility, and ensure that the products they purchase comply with them.

Buyers should also consider the company's product range and specialties, and ensure that the products they purchase are suitable for their intended use. They should request information about the products' materials, properties, and performance, and verify that they meet the required standards and regulations. The company's products may have specific requirements for installation, maintenance, and repair, and buyers should ensure that they have the necessary resources and expertise to meet these requirements.

What types of medical equipment and machinery does Used Device list?

Used Device lists a variety of medical equipment and machinery, including CT Scanners, MRI Scanners, Ultrasound Systems, and X-ray Parts & Instruments.

What is the HS code for medical imaging equipment?

The HS code for medical imaging equipment is 9022.12.

What certifications are typically required for medical equipment and machinery?

Certifications such as CE, FDA, or ISO 13485 are typically required for medical equipment and machinery.

What information should buyers request when sourcing from Used Device?

Buyers should request specifications, samples, and test reports to ensure that the products meet their requirements. They should also verify the company's certifications and request documentation such as user manuals and maintenance records.

What regulations and requirements should buyers be aware of when purchasing medical equipment and machinery?

Buyers should be aware of regulations and requirements related to medical device registration, radiation safety, and electromagnetic compatibility, and ensure that the products they purchase comply with them.

How can buyers ensure that the products they purchase are suitable for their intended use?

Buyers should request information about the products' materials, properties, and performance, and verify that they meet the required standards and regulations. They should also consider the company's product range and specialties, and ensure that the products they purchase are suitable for their intended use.

What are the specific requirements for installation, maintenance, and repair of Used Device's products?

The specific requirements for installation, maintenance, and repair of Used Device's products vary depending on the product and its intended use. Buyers should request information about these requirements and ensure that they have the necessary resources and expertise to meet them.

How can buyers verify the authenticity and quality of Used Device's products?

Buyers can verify the authenticity and quality of Used Device's products by requesting documentation such as test reports, user manuals, and maintenance records. They should also verify the company's certifications and request samples and specifications to ensure that the products meet their requirements.