Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009023553

FEI Number

3009023553

Entity Name

EDEVICE

City/State/Country

Merignac Gironde, FR

Establishment Address

Parc Cadera Sud - Bat P2, Avenue Ariane, Merignac Gironde 33700, FR

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

eDevice (Owner Number: 10036526)

Owner / Operator Contact Address

Parc Cadera Sud - Bat P2, Avenue Ariane, Merignac, FR-33 33700, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

WireX 3G WireX 3G LC WireT HealthGo Mini WireX 4G M-Link HealthGo Micro BridgeD130 Wirex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2011-05-13

Official Correspondent

No official correspondent registered.

US Agent Details

Brett Quas Email: bquas@connectedhcs.com Phone: (262) 3094001

Related Public Records

Same Entity

eDevice

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009023553. Last updated year: 2026. Please use registration number 3009023553 when referencing this establishment in official correspondence.