Asa SRL
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Asa SRL is a medical device manufacturer, with 11 devices listed in FDA GUDID and EUDAMED (FDA Class II) as of 13 Nov 2026.
- Devices
- 11
Registry facts
- Registries
- FDA GUDID 11
- EUDAMED 4
- Device classes
- FDA Class II 11
- Identifiers
- DUNS 429533573
What Asa SRL makes
ASA SRL manufactures non-wearable musculoskeletal infrared phototherapy units designed for therapeutic applications, including models like the Lumolaser, M7, and M-Hi US. These devices target tissue repair and pain relief through controlled infrared light delivery, with variations in power and application settings. Examples include the MiS US, HIRO TT US, and Mphi 7, each tailored for specific clinical use cases.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to applicable medical device standards and reporting requirements.
Catalogue
Search and filter all 11 devicesCompany details
- DUNS number
- 429533573
Frequently asked questions
How many devices does ASA SRL have in the registry?
The registry currently lists 11 devices for ASA SRL. Devices recorded under merged duplicate company entries are counted once.
Which registries list ASA SRL's devices?
Among its 11 most recently registered devices, ASA SRL has devices listed in EUDAMED (4 devices) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ASA SRL's devices fall under?
Among its 11 most recently registered devices, the classes recorded for ASA SRL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ASA SRL in the registry?
The most recently registered devices listed for ASA SRL include M10 F9000318, ASA srl Mphi D, Lumolaser F9000321 and MiS US F9000297.