Data / Medical devices / Mexico / Becton Dickinson De Mexico
Becton Dickinson De Mexico: FDA-registered device maker in CUAUTITLAN, IZCALLI Queretaro, Mexico, 4 510(k) clearances
Becton Dickinson De Mexico is registered with the FDA (registration 9614033) in CUAUTITLAN, IZCALLI Queretaro, Mexico. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated September 2, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9614033
- FEI number
- 1000232458
- Address
- K.M. 37.5 Autopista 55 59 99 8400, CUAUTITLAN, IZCALLI Queretaro, Mexico, 54730
- Owner or operator
- Becton Dickinson and Company (9922032)
- Roles
- Manufacturer
- First device listed
- August 3, 2001
- Registered through
- 2026
- Brand names listed
- BD Blunt Fill NRFit Needle, BD Blunt Fill Needle, BD Blunt Filter NRFit Needle, BD Blunt Filter Needle, BD Hypodermic Needles, BD Hypodermic Syringe, BD Nokor Needle, BD PrecisionGlide Needle and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Aspiration And Injection, Disposable | GAA | 1 | Manufacturer | accessdata.fda.gov |
| Needle, Hypodermic, Single Lumen | FMI | 2 | Manufacturer | accessdata.fda.gov |
| Syringe, Piston | FMF | 2 | Manufacturer | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 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 |
|---|---|---|---|---|---|---|
| September 2, 2015 | K151766 | BD Single Use, Hypodermic Syringe | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| May 13, 2011 | K110771 | BD SINGLE USE, HYPODERMIC SYRINGE | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| July 19, 2002 | K021475 | BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET | FMI | Substantially Equivalent | Bd | accessdata.fda.gov |
| June 11, 1998 | K980987 | BECTON DICKINSON SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Needle, Hypodermic, Single Lumen
- All makers of Syringe, Piston
- All makers of Needle, Aspiration And Injection, Disposable
Updated September 2, 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.