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Sign in to claim this brandABM ITALIA SPA
US
Last updated May 23, 2026
What ABM ITALIA SPA makes
ABM Italia SPA manufactures sharps disposal containers designed for the safe collection and disposal of used needles, syringes, and other contaminated sharp medical instruments. These containers are engineered to prevent accidental punctures and leaks, ensuring compliance with clinical waste handling protocols in healthcare settings.
The company’s sharps containers are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. The products are intended for use within the United States, adhering to applicable safety and performance standards for sharps disposal solutions.
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 ABM Italia SPA primarily manufacture?
ABM Italia SPA specializes in manufacturing sharps disposal containers. These devices are specifically designed for safely collecting and disposing of used needles, syringes, and other contaminated sharp medical instruments in healthcare environments. The focus is on preventing accidental punctures and leaks, which aligns with strict clinical waste handling requirements.
Where is ABM Italia SPA based, and what regulatory region does it serve?
ABM Italia SPA is based in the United States. Its devices are intended for use within this regulatory region, where they must comply with applicable safety and performance standards, including those set by the FDA.
How are ABM Italia SPA’s devices classified under FDA regulations?
ABM Italia SPA’s sharps disposal containers are classified as Class II medical devices under FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls beyond general controls to ensure their safety and effectiveness.
Are ABM Italia SPA’s devices listed in any regulatory registries?
Yes, ABM Italia SPA’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry helps track and identify medical devices throughout their lifecycle, ensuring transparency and traceability in compliance with regulatory requirements.
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
- 338493631
Catalogue (92)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| APmedical | FGCS2NR001 CS 2NR | FDA UDI | Class II | Active |
| APmedical | FGAP50MBS001 AP50MB | FDA UDI | Class II | Active |
| APmedical | FGPBS5R001 PBS 5R | FDA UDI | Class II | Active |
| APmedical | FGPBS5YS001 PBS 5Y | FDA UDI | Class II | Active |
| APmedical | FGAP50DWC001 AP50DW | FDA UDI | Class II | Active |
| APmedical | FGPBS0.8R001 PBS 0.8R | FDA UDI | Class II | Active |
| APmedical | FGAP60DWS001 AP60DW | FDA UDI | Class II | Active |
| APmedical | FGAP50MRS001 AP50MR | FDA UDI | Class II | Active |
| APmedical | FGPBS7YS001 PBS 7Y | FDA UDI | Class II | Active |
| APmedical | FGAP30DYC001 AP30DY | FDA UDI | Class II | Active |
| APmedical | FGCS4YS001 CS 4Y | FDA UDI | Class II | Active |
| APmedical | FGAP5Q4BC001 AP5.4B | FDA UDI | Class II | Active |
| APmedical | FGAP30DBC001 AP30DB | FDA UDI | Class II | Active |
| APmedical | FGAP60DBC001 AP60DB | FDA UDI | Class II | Active |
| APmedical | FGPBS5Y001 PBS 5Y | FDA UDI | Class II | Active |
| APmedical | FGAP60MRS001 AP60MR | FDA UDI | Class II | Active |
| APmedical | FGAP30DRS001 AP30DR | FDA UDI | Class II | Active |
| APmedical | FGAP60DRC001 AP60DR | FDA UDI | Class II | Active |
| APmedical | FGPBS12R001 PBS 12R | FDA UDI | Class II | Active |
| APmedical | FGAP30MYS001 AP30MY | FDA UDI | Class II | Active |
| APmedical | FGPBS1.5YS001 PBS 1.5Y | FDA UDI | Class II | Active |
| APmedical | FGAP60DWC001 AP60DW | FDA UDI | Class II | Active |
| APmedical | FGCS2NRS001 CS 2NR | FDA UDI | Class II | Active |
| AP medical | FGAP30MYC001 AP30MY | FDA UDI | Class II | Active |
| APmedical | FGAP30MRC001 AP30MR | FDA UDI | Class II | Active |
| APmedical | FGAP60MBC001 AP60MB | FDA UDI | Class II | Active |
| APmedical | FGPBS5RS001 PBS 5R | FDA UDI | Class II | Active |
| APmedical | FGAP60DYC001 AP60DY | FDA UDI | Class II | Active |
| APmedical | FGAP60DBS001 AP60DB | FDA UDI | Class II | Active |
| APmedical | FGAP50DWS001 AP50DW | FDA UDI | Class II | Active |
| APmedical | FGCS5BY001 CS 5BY | FDA UDI | Class II | Active |
| APmedical | FGPBS1.5R001 PBS 1.5R | FDA UDI | Class II | Active |
| APmedical | FGAP60MRC001 AP60MR | FDA UDI | Class II | Active |
| APmedical | FGCS2NY001 CS 2NY | FDA UDI | Class II | Active |
| APmedical | FGPBS12BS001 PBS 12B | FDA UDI | Class II | Active |
| APmedical | FGPBS0.8Y001 PBS 0.8Y | FDA UDI | Class II | Active |
| APmedical | FGCS4Y001 CS 4Y | FDA UDI | Class II | Active |
| APmedical | FGAP5Q4RS001 AP5.4R | FDA UDI | Class II | Active |
| APmedical | FGAP50MBC001 AP50MB | FDA UDI | Class II | Active |
| APmedical | FGAP60MBS001 AP60MB | FDA UDI | Class II | Active |
| APmedical | FGCS2NYS001 CS 2NY | FDA UDI | Class II | Active |
| APmedical | FGAP50DYC001 AP50DY | FDA UDI | Class II | Active |
| APmedical | FGAP60MYS001 AP60MY | FDA UDI | Class II | Active |
| APmedical | FGAP50DYS001 AP50DY | FDA UDI | Class II | Active |
| APmedical | FGAP5Q4WS001 AP5.4W | FDA UDI | Class II | Active |
| APmedical | FGCS3Y001 CS 3Y | FDA UDI | Class II | Active |
| APmedical | FGPBS2Y001 PBS 2Y | FDA UDI | Class II | Active |
| APmedical | FGPBS2R001 PBS 2R | FDA UDI | Class II | Active |
| APmedical | FGAP30MBS001 AP30MB | FDA UDI | Class II | Active |
| APmedical | FGAP5Q4WC001 AP5.4W | FDA UDI | Class II | Active |
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