Data / Medical devices / Catheter, Urological (Antimicrobial) And Accessories
Catheter, Urological (Antimicrobial) And Accessories (MJC): 4 FDA-registered makers in 4 countries
4 establishments in 4 countries are registered with the FDA to make Catheter, Urological (Antimicrobial) And Accessories (product code MJC, Class 2, 21 CFR 876.5130). 2 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 10 510(k) clearances under this code, the latest on June 6, 2024, and lists 12 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MJC
- Device class
- 2
- Regulation
- 876.5130
- Medical specialty
- Gastroenterology, Urology
Makers by country
| Country | Makers |
|---|---|
| United States | 1 |
| China | 1 |
| Malaysia | 1 |
| Mexico | 1 |
Makers of Catheter, Urological (Antimicrobial) And Accessories
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| C.R. Bard, Inc. | Covington, GA, United States | Complaint file establishment, Contract sterilizer, Manufacturer, Specification developer | 7 | September 29, 2004 | 0 | 12 | 0 | api.fda.gov |
| Well Lead Medical (hainan) Co., Ltd. | Haikou Hainan, China | Manufacturer | 1 | June 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| Bard Sdn. Bhd. | KULIM Kedah, Malaysia | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Productos Para El Cuidado De La Salud | NOGALES Sonora, Mexico | Contract manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov |
Updated June 6, 2024. 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.