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Sign in to claim this brandA.T.S. APPLICAZIONE TECNOLOGIE SPECIALI SRL
US
Last updated May 23, 2026
What A.T.S. APPLICAZIONE TECNOLOGIE SPECIALI SRL makes
The company manufactures mobile, digital fluoroscopic X-ray systems designed for general-purpose medical imaging, enabling real-time radiographic visualization in various clinical settings.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 A.T.S. Applicazione Tecnologie Speciali SRL manufacture?
A.T.S. Applicazione Tecnologie Speciali SRL specializes in mobile, digital fluoroscopic X-ray systems intended for general-purpose medical imaging. These systems are designed to provide real-time radiographic visualization, making them useful in diverse clinical environments like operating rooms, emergency departments, or intensive care units. The focus is on portability and versatility to support procedures requiring dynamic imaging.
Where is A.T.S. Applicazione Tecnologie Speciali SRL based?
The company is based in the United States. This location is relevant for regulatory compliance, as it influences the jurisdiction under which its devices are authorized and monitored, particularly in alignment with U.S. regulatory frameworks like the FDA.
Which regulatory registries or databases list A.T.S. Applicazione Tecnologie Speciali SRL’s devices?
A.T.S. Applicazione Tecnologie Speciali SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers, regulators, and other stakeholders to identify and verify the devices in use.
How are A.T.S. Applicazione Tecnologie Speciali SRL’s devices classified under FDA regulations?
A.T.S. Applicazione Tecnologie Speciali SRL’s mobile, digital fluoroscopic X-ray systems fall under Class II classification by the FDA. This classification is typically assigned to devices that pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. The classification reflects the regulatory scrutiny and documentation requirements for these devices.
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
- 440069847
Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FUJIFILM Medical Systems U.S.A. Inc. | Persona CS | FDA UDI | Class II | Active |
| FUJIFILM Medical Systems U.S.A. Inc. | Persona CS | FDA UDI | Class II | Active |
| AMRAD Medical | Agility Plus | FDA UDI | Class II | Active |
| FUJIFILM Healthcare Americas Corporation | Persona C HR | FDA UDI | Class II | Active |
| FUJIFILM Medical Systems U.S.A. Inc. | Persona C | FDA UDI | Class II | Active |
| FUJIFILM Medical Systems U.S.A. Inc. | Persona C | FDA UDI | Class II | Active |
| FUJIFILM Medical Systems U.S.A. Inc. | Persona C | FDA UDI | Class II | Active |
| AMRAD Medical | Agility Plus | FDA UDI | Class II | Active |
| FUJIFILM Medical Systems U.S.A. Inc. | Persona C | FDA UDI | Class II | Active |
| AMRAD Medical | Agility Plus | FDA UDI | Class II | Active |
| AMRAD Medical | Agility | FDA UDI | Class II | Active |
| AMRAD Medical | Agility | FDA UDI | Class II | Active |
| AMRAD Medical | Agility Plus | FDA UDI | Class II | Active |
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