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Sign in to claim this brandTechnomed Engineering B.V.
US
Last updated May 24, 2026
What Technomed Engineering B.V. makes
Technomed Engineering B.V. manufactures single-use and reusable electrodes and probes for electromyography (EMG) and nerve stimulation, including subdermal needle electrodes, EMG needle electrodes, and nerve-locating probes. Their portfolio also includes analytical cutaneous electrodes and endotracheal tube electrodes for diagnostic and monitoring applications, as well as reusable electrical connection cables for medical devices.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Technomed Engineering B.V. is based in 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 Technomed Engineering B.V. manufacture?
Technomed Engineering B.V. specializes in electrodes and probes primarily used for electromyography (EMG) and nerve stimulation. Their product range includes single-use items like subdermal needle electrodes, EMG needle electrodes, nerve-locating probes, and endotracheal tube electrodes. They also produce reusable electrical connection cables and analytical cutaneous electrodes for diagnostic and monitoring purposes, ensuring compatibility with various medical applications.
Where is Technomed Engineering B.V. based?
Technomed Engineering B.V. is headquartered in the United States. While the company operates globally through its product distribution, its primary location is within the US.
Which regulatory registries list Technomed Engineering B.V.’s devices?
Technomed Engineering B.V.’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 US, ensuring transparency and traceability for healthcare providers and regulators.
How are Technomed Engineering B.V.’s devices classified under FDA regulations?
Technomed Engineering B.V.’s devices fall under Class II classification according to FDA regulations. This classification applies to products that generally pose moderate risk and require special controls—such as performance standards or post-market surveillance—to ensure their safety and effectiveness.
What distinguishes Technomed Engineering B.V.’s reusable and single-use devices?
Technomed Engineering B.V. manufactures both single-use and reusable devices to cater to different clinical needs. Single-use items like EMG needle electrodes and nerve-locating probes are designed for one-time use to minimize infection risks, while reusable devices—such as electrical connection cables—are engineered for durability and repeated sterilization, balancing cost efficiency with safety standards.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- technomed.nl
- —
- —
- [email protected]
- Phone
- +31434086868
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 418415568
Catalogue (192)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Neuroguard | S46-937/02 | FDA UDI | Class II | Active |
| Natus | 027722 | FDA UDI | Class II | Active |
| Neurosign V4 | 5883-00 | FDA UDI | Class II | Active |
| Consolidated Neuro Supply | S44-937/02 | FDA UDI | Class II | Active |
| Cadwell | 202452-000 | FDA UDI | Class II | Active |
| Technomed Europe | TE/D12-301 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/C24-834/99 | FDA UDI | Class II | Unknown |
| Technomed Europe | MP214-3.0/1 | FDA UDI | Class II | Active |
| Cadwell | 302911-000 | FDA UDI | Class II | Active |
| Technomed Europe | TE/S50725-004-C | FDA UDI | Class II | Active |
| Cadwell | 302885-000-GP2 | FDA UDI | Class II | Active |
| Cadwell | 302860-000-GP2 | FDA UDI | Class II | Unknown |
| Neurosign V4 | 4017-00 | FDA UDI | Class II | Unknown |
| Neurosign V4 | 5887-00 | FDA UDI | Class II | Active |
| Neurosign V4 | 4202-00 | FDA UDI | Class II | Unknown |
| Neuroradium | NR-1025 | FDA UDI | Class II | Active |
| Technomed Europe | TE/L3740-335 | FDA UDI | Class II | Active |
| Technomed Europe | TE/L2530-335 | FDA UDI | Class II | Active |
| Cadwell | 302918-000 | FDA UDI | Class II | Active |
| Pinnacle | 4010-00 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/S50715-003 | FDA UDI | Class II | Active |
| Natus | 027721 | FDA UDI | Class II | Active |
| Technomed Europe | TE/L5050-335 | FDA UDI | Class II | Active |
| Neurosign V4 | 4012-00 | FDA UDI | Class II | Unknown |
| Natus | 027781 | FDA UDI | Class II | Active |
| Technomed Europe | TE/B50600-004 | FDA UDI | Class II | Unknown |
| Neurosign | NM-Kit 1 | FDA UDI | Class II | Active |
| Cadwell | 302885-000 | FDA UDI | Class II | Active |
| Spineology | 312-0017 | FDA UDI | Class II | Active |
| Natus | 027726 | FDA UDI | Class II | Active |
| Cadwell | 302914-000-GP2 | FDA UDI | Class II | Active |
| Technomed Europe | TE/S50715-004 | FDA UDI | Class II | Active |
| Neuroradium | NR-2008 | FDA UDI | Class II | Active |
| Technomed Europe | TE/C24-934/99 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/S50725-002 | FDA UDI | Class II | Active |
| Neuroguard | K50430-015 | FDA UDI | Class II | Active |
| Neurosign V4 | 4200-00 | FDA UDI | Class II | Active |
| Technomed Europe | TE/S50723-001 | FDA UDI | Class II | Active |
| Technomed Europe | TE/S50725-004 | FDA UDI | Class II | Active |
| Technomed Europe | TE/S50725-001-C | FDA UDI | Class II | Active |
| Cadwell | 302916-000 | FDA UDI | Class II | Active |
| Cadwell | 302912-000 | FDA UDI | Class II | Active |
| Neurosign V4 | 4024-00 | FDA UDI | Class II | Unknown |
| Natus | 038315 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/B50035-004 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/B50600-001 | FDA UDI | Class II | Unknown |
| Neurosign V4 | 4201-00 | FDA UDI | Class II | Active |
| Biosense Webster | C6FFMST10 | FDA UDI | Class II | Unknown |
| Technomed Europe | TE/S50722-003 | FDA UDI | Class II | Active |
| Technomed Europe | BTP3.0-100/1 | FDA UDI | Class II | Active |
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