Data / Medical devices / India / Mediplus (india) Limited
Mediplus (india) Limited: FDA-registered device maker in Bahadurgarh Haryana, India, 1 510(k) clearance
Mediplus (india) Limited is registered with the FDA (registration 3005956311) in Bahadurgarh Haryana, India. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 25, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005956311
- Address
- 1261-1262, M.I.E. Part B, Bahadurgarh-124507 Haryana (India), Bahadurgarh Haryana, India, 124507
- Owner or operator
- Mediplus (India) Limited (10085480)
- Roles
- Manufacturer
- First device listed
- June 23, 2022
- Registered through
- 2026
- Brand names listed
- PLUSKI SAFE1 SAFETY IV CATHETER
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 25, 2022 | K210037 | Pluski Safe 1 Safety IV Catheter | FOZ | Substantially Equivalent | Mediplus (India) Limited | accessdata.fda.gov |
Compare with other makers
Updated March 25, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.