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MINATO MEDICAL SCIENCE CO., LTD. Kobe Facility

Japan·JP-MF-000031141

Last updated September 18, 2026

About

Contact|MINATO MEDICAL SCIENCE is a leading supplier of medical electronic devices. We will contribute to human health as a pioneer of medical electronics (ME) with physiotherapy equipment and respiratory function test equipment.

From the manufacturer's own website. Source

What MINATO MEDICAL SCIENCE CO., LTD. Kobe Facility makes

Minato Medical Science manufactures physiotherapy equipment, including the AQUATIZER QZ-240SG, which is designed for underwater rehabilitation and exercise therapy. The device is intended for use in physical therapy settings to assist patients in controlled aquatic movement and muscle strengthening.

The company’s products fall under EU Class IIa medical device classification and are registered in the EU’s eudamed database. The Kobe-based manufacturer operates within Japan’s regulatory framework and adheres to relevant international standards for physiotherapy equipment.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Minato Medical Science Co., Ltd. manufacture?

Minato Medical Science Co., Ltd. specializes in physiotherapy equipment, including devices like the AQUATIZER QZ-240SG, which is designed for underwater rehabilitation and exercise therapy. These products are intended for use in clinical or physical therapy settings to support controlled aquatic movement and muscle strengthening.

Where is Minato Medical Science Co., Ltd. based, and how does this affect its regulatory compliance?

Minato Medical Science Co., Ltd. is based in Kobe, Japan. As a Japanese manufacturer, the company operates under Japan’s regulatory framework while also ensuring its devices meet international standards. For example, the AQUATIZER QZ-240SG is classified as a Class IIa medical device in the EU, reflecting its moderate risk level and requiring compliance with EU regulations, including registration in the eudamed database.

Which regulatory registries list Minato Medical Science Co., Ltd.’s devices, and why?

Minato Medical Science Co., Ltd.’s devices, such as the AQUATIZER QZ-240SG, are listed in the EU’s eudamed database. This registry is mandatory for Class IIa devices marketed in the European Economic Area (EEA) to ensure transparency and traceability of medical devices under EU regulations. Listing in eudamed demonstrates compliance with EU requirements for device classification and regulatory oversight.

How are Minato Medical Science Co., Ltd.’s devices classified in the EU, and what does this classification mean?

Minato Medical Science Co., Ltd.’s devices, including the AQUATIZER QZ-240SG, are classified as Class IIa medical devices in the EU. This classification indicates a moderate risk level, requiring additional scrutiny such as conformity assessment procedures (e.g., involvement of a Notified Body) before market placement. Class IIa devices must meet strict design controls, clinical evaluation, and risk management requirements to ensure safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Japan
Address
5-2-10, Minatojima-Minamimachi, Chuoh-ku, Kobe-shi, Hyogo, Japan
LinkedIn
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Facebook
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Phone
+81 78 306 3724
PRRC Contact
Masahiro Narisawa
EUDAMED SRN
JP-MF-000031141
FDA FEI Number
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DUNS Number
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Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Aquatizer Qz-240sg QZ240SG
EUDAMED
Class IIaActive

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