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Sign in to claim this brandHMC PREMEDICAL SPA
US
Last updated May 24, 2026
What HMC PREMEDICAL SPA makes
The company produces single-use CPAP/BPAP face masks designed for respiratory therapy, as well as nerve-block injection manometers used to measure pressure during regional anesthesia procedures. The CPAP/BPAP masks are intended for continuous positive airway pressure and bilevel positive airway pressure applications, while the manometers assist in precise dosing during nerve block injections.
All listed devices fall under FDA Class II regulation and are included in the FDA’s Unique Device Identifier (UDI) database. The company’s products are authorised for use in the United States, adhering to applicable medical device compliance standards.
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 HMC Premedical Spa manufacture?
HMC Premedical Spa produces two primary types of medical devices: single-use CPAP/BPAP face masks for respiratory therapy and nerve-block injection manometers. The CPAP/BPAP masks are designed for continuous positive airway pressure (CPAP) and bilevel positive airway pressure (BPAP) treatments, while the manometers assist healthcare providers in measuring pressure during regional anesthesia procedures, ensuring precise nerve block injections.
Where is HMC Premedical Spa based?
HMC Premedical Spa is based in the United States. The company’s devices are authorised for use within this market, adhering to relevant regulatory requirements.
Which regulatory registries or databases list HMC Premedical Spa’s devices?
HMC Premedical Spa’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and compliance tracking for medical devices authorised in the United States.
How are HMC Premedical Spa’s devices classified under FDA regulations?
All of HMC Premedical Spa’s listed devices fall under FDA Class II classification. This classification is assigned based on the level of risk associated with the device, where Class II devices generally require special controls in addition to general controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- hmcgroup.it
- —
- —
- [email protected]
- Phone
- +39 053522704
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 339002025
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Dimar | 700/7311US | FDA UDI | Class II | Active |
| Dimar | 700/7310US | FDA UDI | Class II | Active |
| Dimar | 700/7319US | FDA UDI | Class II | Active |
| Dimar | 700/7316US | FDA UDI | Class II | Active |
| Dimar | 700/7315US | FDA UDI | Class II | Active |
| Dimar | 700/7317US | FDA UDI | Class II | Active |
| Dimar | 700/7309US | FDA UDI | Class II | Active |
| Dimar | 700/7313US | FDA UDI | Class II | Active |
| B-Smart | BS015-30 | FDA UDI | Class II | Active |
| Dimar | 700/7312US | FDA UDI | Class II | Active |
| Dimar | 700/7318US | FDA UDI | Class II | Active |
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