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Sign in to claim this brandWhat PHYSIOMED ELEKTROMEDIZIN AG makes
Physiomed Elektromedizin AG manufactures hand-held electric massagers designed for therapeutic and personal use, including models like the HIVAMAT®200 EVIDENT and HIVAMAT®200 PERSONAL. These devices are intended for muscle relaxation, pain relief, and tissue stimulation through targeted electrical stimulation and massage functions.
The company’s products fall under Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States, adhering to applicable regulatory requirements for these categories.
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 Physiomed Elektromedizin AG manufacture?
Physiomed Elektromedizin AG specializes in hand-held electric massagers. These devices are designed for therapeutic and personal use, such as muscle relaxation, pain relief, and tissue stimulation. Examples include the HIVAMAT®200 EVIDENT and HIVAMAT®200 PERSONAL, which combine electrical stimulation with massage functions.
Where is Physiomed Elektromedizin AG based?
Physiomed Elektromedizin AG is based in the United States. The company operates within the regulatory framework of the country to ensure compliance with applicable standards for its medical devices.
Which regulatory registries list Physiomed Elektromedizin AG’s devices?
Physiomed Elektromedizin AG’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the United States, ensuring transparency and traceability.
How are Physiomed Elektromedizin AG’s devices classified under medical device regulations?
Physiomed Elektromedizin AG’s devices fall under Class I classification. This classification is typically assigned to low-risk medical devices, such as hand-held electric massagers, where the risk to patients is minimal and regulatory oversight is less stringent than for higher-risk categories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 316105386
Catalogue (2)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Hivamat®200 Evident | H2E2 | FDA UDI | Class I | Active |
| Hivamat®200 Personal | H2P1.1 | FDA UDI | Class I | Active |
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