East End Medical I, LLC
United StatesFDA applicant, unverified
- Devices
- 5
What East End Medical I, LLC makes
East End Medical I, LLC manufactures vascular introducer systems, including the SafeCross Vascular Introducer System and the SafeCross Transseptal Puncture and Introducer System. These devices are designed for use in interventional procedures, such as transseptal punctures and vascular access.
The company’s products are classified as Class II medical devices and are listed under FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
SafeCross Vascular Introducer System (4001) Ref K240600
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 118148023
- [email protected]
- Phone
- 9542406694
Frequently asked questions
How many devices does East End Medical I, LLC have in the registry?
The registry currently lists 5 devices for East End Medical I, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list East End Medical I, LLC's devices?
Among its 5 most recently registered devices, East End Medical I, LLC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do East End Medical I, LLC's devices fall under?
Among its 5 most recently registered devices, the classes recorded for East End Medical I, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from East End Medical I, LLC in the registry?
The most recently registered devices listed for East End Medical I, LLC include SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System 3002, SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System 3003, SafeCross Transseptal RF Puncture and Steerable Balloon Introducer System 3001 and SafeCross Vascular Introducer System (4001).