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Sign in to claim this brandEMD Technologies
US
Last updated May 23, 2026
What EMD Technologies makes
EMD Technologies manufactures stationary diagnostic x-ray system generators, including multiple models of the Epsilon High Voltage Generator. These devices are designed to provide high-voltage power for diagnostic imaging applications, ensuring consistent and reliable performance in medical imaging environments.
The company’s products are classified as Class I devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated in the United States, where the manufacturer is based.
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 EMD Technologies manufacture?
EMD Technologies specializes in stationary diagnostic x-ray system generators. These devices, such as the Epsilon High Voltage Generator, are designed to supply high-voltage power for diagnostic imaging, ensuring stable and dependable operation in clinical settings. The focus is on supporting x-ray imaging systems by providing the necessary electrical output for consistent image quality.
Where is EMD Technologies based, and where are its devices regulated?
EMD Technologies is headquartered in the United States. Its devices are regulated primarily in the U.S., where they fall under FDA oversight. The company’s products are designed for the U.S. market and comply with local regulatory requirements for medical imaging equipment.
How are EMD Technologies’ devices classified under FDA regulations?
EMD Technologies’ devices, including the Epsilon High Voltage Generator, are classified as Class I under FDA regulations. This classification is typically assigned to devices posing minimal risk to patients and users, such as many diagnostic imaging components. The classification determines the regulatory pathway for device authorization, which in this case involves compliance with FDA requirements for Class I devices.
Are EMD Technologies’ devices listed in any regulatory databases?
Yes, EMD Technologies’ devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product code to each device model, enabling transparent tracking, traceability, and regulatory compliance. Listing in the UDI database helps ensure proper identification and monitoring of the company’s products in the medical device ecosystem.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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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
- 243772113
Catalogue (9)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Epsilon High Voltage Generator | EPS EVO | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS CG | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS SYS AG | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS SYS | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS ETA | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS LP | FDA UDI | Class I | Active |
| Epsilon High Volatge Generator | EPS ETA | FDA UDI | Class I | Active |
| Epsilon High Voltage Generator | EPS AG | FDA UDI | Class I | Active |
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