Fresenius Vial S.A.S.

FDA Device Registration & Listing · Brezins Isere, FR · Registration 3000240707

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3000240707
FEI Number
3000240707
Entity Name
Fresenius Vial S.A.S.
City/State/Country
Brezins Isere, FR
Establishment Address
Le Grand Chemin, Brezins Isere F-38590, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Fresenius Kabi AG (Owner Number: 9027285)
Owner / Operator Contact Address
Else-Kroner-Str. 1, 61352 Bad Homburg, DE-NOTA NONE, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

VSS Vigilant Master Med Agilia SP Infusion System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PHC Infusion Safety Management Software General Hospital Class 2 880.5725 2022-05-09
MRZ Accessories, Pump, Infusion General Hospital Class 2 880.5725 2022-08-05
FRN Pump, Infusion General Hospital Class 2 880.5725 2022-08-05
FPA Set, Administration, Intravascular General Hospital Class 2 880.5440 2022-08-05

Official Correspondent

No official correspondent registered.

US Agent Details

Rhoda Lynn Valera Email: rhoda.valera@fresenius-kabi.com Phone: (847) 5502929

Related Public Records

Same Entity

Fresenius Kabi AG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3014732157 Fresenius Kabi USA, LLC North Andover, MA, US
3004634229 FRESENIUS HEMOCARE GMBH Friedberg Hesse, DE
9611902 Fenwal France S.A.S. Lacs Indre, FR
9681819 FRESENIUS KABI DEUTSCHLAND GMBH BAD HERSFELD Hesse, DE
3008810357 Clinico Medical Sp. z o.o. Blonie/Miekinia Dolnoslaskie, PL

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K913718 Abbott Laboratories PANCRETEC I.V. MODEL 5000 INFUS DEVICE, MODIFIED 1991-10-30
K840616 Advanced Bio Systems, Inc. MINI-PUMP U-100 1984-03-30
K850183 Deltec Systems, Inc. CADD-VT, 5300 AMBULATORY INFUSION PUMP W/3050, 50M 1985-03-13
K221518 Np Medical NP Medical nCompass Extension Set with Stabilizing Base 2022-11-03
K953474 Medikmark, Inc. IV START KIT 1995-10-02

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2023 Fresenius Kabi USA, LLC 2
Ivenix Infusion System (IIS), LVP Software; LVP-SW-0004 version 5.2.0
Z-0001-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Single Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product Codes: 2M8151, 2M8161, and 2M9161.
Z-0002-2011 Baxter Healthcare Corp. Rt. 2
Baxter Colleague Triple Channel Volumetric Infusion Pumps. Baxter Healthcare Corporation, Medication Delivery Division. Product codes: 2M8153, and 2M8163.
Z-0005-2025 Zyno Medical LLC 2
Z-800 Infusion System, Model Numbers Z-800, Z-800F, Z-800W, Z-800WF; Software Version: Z-800 6.1.01 and 6-1.07z; Z-800F 4.1.02 and 4.1.08z; Z-800W 3.1.32 and 3.1.64z, Z-800WF 3.1.32 and 3.1.64z
Z-0006-2011 CareFusion Corporation 2
CareFusion Alaris PC Unit Model 8015 (formerly Medley PC Unit): Alaris PC Units (Model 8015) with logic board part number TC10005522 manufactured and serviced between December 20, 2008 and May 6, 2009; and Alaris PC Units (with logic board part number TC10005572 manufactured and serviced between May 7, 2009 and September 8, 2009. For use with Alaris infusion and monitoring systems.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3000240707. Last updated year: 2026. Please use registration number 3000240707 when referencing this establishment in official correspondence.
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