Tri-Ject Intl. Corp.
Country not established
- Devices
- 1
What Tri-Ject Intl. Corp. makes
Tri-Ject Intl. Corp. manufactures the E.N.S.I. Syringe, a pre-filled, single-use syringe designed for precise medication delivery in clinical settings.
The E.N.S.I. Syringe is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
E.N.S.I. Syringe Ref K000572
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tri-Ject Intl. Corp. have in the registry?
The registry currently lists 1 device for Tri-Ject Intl. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-Ject Intl. Corp.'s devices?
Among its 1 most recently registered device, Tri-Ject Intl. Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Tri-Ject Intl. Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tri-Ject Intl. Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri-Ject Intl. Corp. in the registry?
The most recently registered devices listed for Tri-Ject Intl. Corp. include E.N.S.I. SYRINGE.