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Becton, Dickinson & Co.

Also registered as BECTON DICKINSON, Becton, Dickinson Company

Country not established FDA establishment FEI 1111096

Devices
203
Registrations
FDA
FDA recalls
0

Catalogue203

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Company details

FDA FEI number
1111096
Address
250 Schilling Cir, Cockeysville, MD, 21030

Frequently asked questions

How many devices does BECTON, DICKINSON & CO. have in the registry?

The registry currently lists 203 devices for BECTON, DICKINSON & CO.. Devices recorded under merged duplicate company entries are counted once.

Which registries list BECTON, DICKINSON & CO.'s devices?

Among its 50 most recently registered devices, BECTON, DICKINSON & CO. has devices listed in FDA 510(k) (50 devices).

What risk classes do BECTON, DICKINSON & CO.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for BECTON, DICKINSON & CO.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from BECTON, DICKINSON & CO. in the registry?

The most recently registered devices listed for BECTON, DICKINSON & CO. include BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-VANCOMYCIN GRAM POSITIVE, BD Veritor System for the Rapid Detection of Flu A + B CLIA waived kit, BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM-PIPERCILLIN (GN) 0.5-128 UG/ML and BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.