Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012776242

FEI Number

3012776242

Entity Name

ARTHESYS

City/State/Country

SACLAY Ile-de-France, FR

Establishment Address

4 RUE RENE RAZEL, SACLAY Ile-de-France 91400, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ARTHESYS (Owner Number: 10095459)

Owner / Operator Contact Address

4 RUE RENE RAZEL, SACLAY, FR-IDF 91400, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Y-Cross Y Connector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DTL	Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4290	2026-03-16

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

ARTHESYS

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K915301	Advance Medical Designs, Inc.	ADVANCE STOPCOCK/HIGH PRESSURE STOPCOCK	1992-12-11

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9612152	ELCAM MEDICAL A.C.A.L.	D.N. MEROM HAGALIL Northern, IL
2184009	MEDTRONIC PERFUSION SYSTEMS	Minneapolis, MN, US
1450662	Isomedix Operations, Inc.	Libertyville, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012776242. Last updated year: 2026. Please use registration number 3012776242 when referencing this establishment in official correspondence.