Data / Medical devices / Brazil / Becton Dickinson Industrias Cirurgicas, Ltda.
Becton Dickinson Industrias Cirurgicas, Ltda.: FDA-registered device maker in JUIZ DE FORA Minas Gerais, Brazil, 1 510(k) clearance
Becton Dickinson Industrias Cirurgicas, Ltda. is registered with the FDA (registration 9610048) in JUIZ DE FORA Minas Gerais, Brazil. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 27, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9610048
- FEI number
- 3002806482
- Address
- Avenida Presidente Juscelino Kubitschek 273 Francisco Bernardino, JUIZ DE FORA Minas Gerais, Brazil, 36081-000
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Manufacturer
- First device listed
- December 13, 2010
- Registered through
- 2026
- Brand names listed
- BD Angiocath IV Catheter, BD Insyte IV Catheter, Glass LOR Syringe, Glasspak Syringe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FOZ | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 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 |
|---|---|---|---|---|---|---|
| July 27, 2015 | K151698 | BD Angiocath IV Catheter, BD Insyte IV Catheter | FOZ | Substantially Equivalent | Becton Dickinson Infusion Therapy Systems, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Piston
- All makers of Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Updated July 27, 2015. 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.