Hudi Pharma SRL
ItalyFDA applicant, unverified FDA FEI 3015686320
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Hudi Pharma SRL makes
Hudi Pharma Srl manufactures vaginal suppositories containing hyaluronic acid in two strengths: 5 mg and 10 mg. These devices are designed for topical administration in the vaginal area.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg) Ref K260007
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015686320
- DUNS number
- 440408341
- Address
- Piazza Giuseppe Grandi 19, Milano
Frequently asked questions
How many devices does Hudi Pharma Srl have in the registry?
The registry currently lists 2 devices for Hudi Pharma Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hudi Pharma Srl's devices?
Among its 2 most recently registered devices, Hudi Pharma Srl has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Hudi Pharma Srl's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hudi Pharma Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hudi Pharma Srl in the registry?
The most recently registered devices listed for Hudi Pharma Srl include Hyaluronic Acid Vaginal Suppository (HA 10 mg) and Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA 10 mg).