Data / Medical devices / Brazil / Becton Dickinson Ind. Cirurgicas Ltda.
Becton Dickinson Ind. Cirurgicas Ltda.: FDA-registered device maker in CURITIBA Parana, Brazil, 1 510(k) clearance
Becton Dickinson Ind. Cirurgicas Ltda. is registered with the FDA (registration 3003916417) in CURITIBA Parana, Brazil. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 27, 2016. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3003916417
- FEI number
- 3003910417
- Address
- Rua Cyro Correia Pereira 550, CURITIBA Parana, Brazil, 81170-230
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Contract sterilizer, Manufacturer
- First device listed
- April 15, 2016
- Registered through
- 2026
- Brand names listed
- BD Angiocath IV Catheter, BD Insyte IV Catheter, Eclipse
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Contract sterilizer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 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 |
|---|---|---|---|---|---|---|
| May 27, 2016 | K161170 | BD Eclipse Hypodermic Needle | FMI | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
Compare with other makers
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- All makers of Needle, Hypodermic, Single Lumen
Updated May 27, 2016. 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.