BD Medical-Medical Surgical Systems
Country not established
- Devices
- 2
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What BD Medical-Medical Surgical Systems makes
Bd Medical-Medical Surgical Systems makes protectors, injectors, and connectors.
These devices are Class II medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Bd Eclipse Hypodermic Needle Ref K010188
Regimes: 510(k) Registry: 510(k)Protector, Injector, Connector Ref K120384
Regimes: 510(k) Registry: 510(k)
FDA recalls
2010
- 24 Jun 2010 Z-0822-2011 Unclassified (pre-2012) Terminated Blades may contain defects at the blade tip or cutting edge.
Frequently asked questions
How many devices does Bd Medical-Medical Surgical Systems have in the registry?
The registry currently lists 2 devices for Bd Medical-Medical Surgical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bd Medical-Medical Surgical Systems's devices?
Among its 2 most recently registered devices, Bd Medical-Medical Surgical Systems has devices listed in FDA 510(k) (2 devices).
What risk classes do Bd Medical-Medical Surgical Systems's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bd Medical-Medical Surgical Systems's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Bd Medical-Medical Surgical Systems?
FDA recall records list 1 recall initiated by Bd Medical-Medical Surgical Systems, the most recent initiated on 24 Jun 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Bd Medical-Medical Surgical Systems in the registry?
The most recently registered devices listed for Bd Medical-Medical Surgical Systems include BD ECLIPSE HYPODERMIC NEEDLE and PROTECTOR, INJECTOR, CONNECTOR.