Data / Medical devices / Mexico / Mirsa Manufactura Inspeccion Y Retrabajo
Mirsa Manufactura Inspeccion Y Retrabajo: FDA-registered device maker in REYNOSA Tamaulipas, Mexico, 1 510(k) clearance
Mirsa Manufactura Inspeccion Y Retrabajo is registered with the FDA (registration 3036757319) in REYNOSA Tamaulipas, Mexico. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 7, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3036757319
- Address
- Privada Martel S/N Lote 1 Y 2 Parque Industrial Reynosa Seccion Norte, REYNOSA Tamaulipas, Mexico, 88788
- Owner or operator
- MIRSA MANUFACTURA INSPECCION Y RETRABAJO (10092811)
- Roles
- Repackager or relabeler
- First device listed
- February 20, 2025
- Registered through
- 2026
- Brand names listed
- MicroWash
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Specimen Mailer And Storage, Non-Sterile | NNK | 1 | Repackager or relabeler | accessdata.fda.gov |
| Pump, Nebulizer, Manual | EPN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Saline, Vascular Access Flush | NGT | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| February 7, 2013 | K121050 | 0.9% SODIUM CHLORIDE INJECTION USP BD POSIFLUSH FLUSH SYRINGE, SF FLUSH SYRINGE | NGT | Substantially Equivalent | Becton, Dickinson & CO | accessdata.fda.gov |
Compare with other makers
- All makers of Pump, Nebulizer, Manual
- All makers of Saline, Vascular Access Flush
- All makers of Container, Specimen Mailer And Storage, Non-Sterile
Updated February 7, 2013. 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.