Is this your brand? Sign in to claim ownership.
Sign in to claim this brandHAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H.
US
Last updated May 31, 2026
What HAKO-MED Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H. makes
The company produces interferential electrical stimulation systems designed for therapeutic applications, including pain management and muscle stimulation. These devices deliver alternating electrical currents to promote tissue healing and improve patient mobility through targeted electrical interference.
The portfolio consists of Class II medical devices, which are regulated under the FDA’s Unique Device Identifier (UDI) system. These products are listed in the FDA’s UDI database, adhering to U.S. regulatory requirements for Class II devices. The manufacturer operates from the United States.
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 Hako-Med Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H. manufacture?
Hako-Med specializes in producing interferential electrical stimulation systems, which are designed for therapeutic uses like pain management and muscle stimulation. These devices work by delivering alternating electrical currents to encourage tissue healing and enhance patient mobility through controlled electrical interference.
Where is Hako-Med Herstellung + Vertrieb von medizinisch-technischen Geräten G.m.b.H. based?
The company is based in the United States, where it operates as a manufacturer of medical devices.
Which regulatory registries list Hako-Med’s devices?
Hako-Med’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, as they fall under the U.S. regulatory classification system for medical devices.
How are Hako-Med’s devices classified under U.S. regulations?
Hako-Med’s devices are classified as Class II under FDA regulations. This classification applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, including compliance with the UDI system.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 331405535
Catalogue (2)
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.