Mankind Pharma Limited
IndiaFDA applicant, unverified FDA FEI 3009083745
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Mankind Pharma Limited makes
Mankind Pharma Limited manufactures sodium chloride inhalation solutions in USP-compliant concentrations of 0.9%, 3%, and 7% for respiratory therapy.
These inhalation solutions are classified as Class II medical devices under FDA regulations and are recorded in the 510(k) clearance database. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009083745
- Address
- Unit-III, Village Kunja, Paonta Sahib, Sirmaur Himachal Pradesh
Frequently asked questions
How many devices does Mankind Pharma Limited have in the registry?
The registry currently lists 1 device for Mankind Pharma Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mankind Pharma Limited's devices?
Among its 1 most recently registered device, Mankind Pharma Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Mankind Pharma Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mankind Pharma Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mankind Pharma Limited in the registry?
The most recently registered devices listed for Mankind Pharma Limited include Sodium Chloride Inhalation Solution, USP 0.9%, 3% & 7%.