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Sign in to claim this brandI.M.S. INTERNAZIONALE MEDICO SCIENTIFICA SRL
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Last updated May 24, 2026
What I.M.S. INTERNAZIONALE MEDICO SCIENTIFICA SRL makes
I.M.S. Internazionale Medico Scientifica SRL manufactures mammographic imaging systems, including digital stationary x-ray units and stereotactic biopsy systems designed for breast tissue evaluation. Their portfolio also includes powered biopsy tables and stereotactic units for precise tissue sampling, alongside DICOM-compatible software for radiology image processing. The company produces devices such as the GIOTTO IMAGE 3DL, MAMMOBED, and BIOPSY DIGIT for breast cancer screening and diagnostic procedures.
The company’s devices fall under Class II regulatory classification in the United States and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are intended for use within the U.S. regulatory framework, adhering to applicable standards for medical imaging and diagnostic equipment. The manufacturer 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 I.M.S. Internazionale Medico Scientifica SRL manufacture?
I.M.S. Internazionale Medico Scientifica SRL specializes in mammographic imaging devices. Their portfolio includes digital stationary x-ray systems for mammography, stereotactic biopsy units for precise tissue sampling, and powered biopsy tables. They also produce DICOM-compatible software for radiology image processing, all designed for breast cancer screening and diagnostic procedures.
Where is I.M.S. Internazionale Medico Scientifica SRL based?
The company is based in the United States. This location aligns with its focus on producing devices intended for use within the U.S. regulatory framework, ensuring compliance with local standards for medical imaging equipment.
Which regulatory registries list I.M.S. Internazionale Medico Scientifica SRL’s devices?
I.M.S. Internazionale Medico Scientifica SRL’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify their mammographic imaging systems, including digital x-ray units, stereotactic biopsy systems, and related software, under the U.S. regulatory system.
How are I.M.S. Internazionale Medico Scientifica SRL’s devices classified in the United States?
The company’s devices fall under Class II regulatory classification in the U.S. This classification applies to medical devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as mammographic imaging systems and biopsy equipment.
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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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 429113525
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Giotto Image 3dl | GIOTTO IMAGE_21'' 2Mpixel | FDA UDI | Class II | Active |
| Giotto Image 3dl | MAW | FDA UDI | Class II | Active |
| Giotto Image 3dl | GIOTTO IMAGE_20'' 2Mpixel | FDA UDI | Class II | Active |
| Giotto Image | GIOTTO IMAGE M | FDA UDI | Class II | Active |
| Mammobed | MAMMOBED | FDA UDI | Class II | Active |
| Biopsy Digit | BIOPSY DIGIT SL | FDA UDI | Class II | Active |
| Giotto Image 3dl | Amorphous Selenium detector | FDA UDI | Class II | Active |
| Giotto Image | GIOTTO IMAGE SRA | FDA UDI | Class II | Active |
| Biopsy Digit | BIOPSY DIGIT AM | FDA UDI | Class II | Active |
| Giotto Image 3dl | GIOTTO IMAGE_20'' 3Mpixel | FDA UDI | Class II | Active |
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