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Becton, Dickinson & Co., (Bd)

Also registered as Becton Dickinson Inc. (Bd)

Country not established FDA establishment FEI 1024879

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
1024879
Address
1575 Airport Rd, SUMTER, SC, 29153

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Becton, Dickinson & Company (BD) Plymouth Devon · GB FEI 3002806485

Frequently asked questions

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

The registry currently lists 1 device for BECTON, DICKINSON & CO., (BD). Devices recorded under merged duplicate company entries are counted once.

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

Among its 1 most recently registered device, BECTON, DICKINSON & CO., (BD) has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for BECTON, DICKINSON & CO., (BD)'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for BECTON, DICKINSON & CO., (BD) include CentroVena Central Venous Catheter (CVC) with the CentroVena One Insertion System.

Which FDA establishments are linked to BECTON, DICKINSON & CO., (BD)?

1 FDA establishment is linked to BECTON, DICKINSON & CO., (BD) in the registry; they are listed on the company page.

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.