GVS SPA

FDA Device Registration & Listing · Borgocarbonara Mantova, IT · Registration 9614854

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
9614854
FEI Number
3003824461
Entity Name
GVS SPA
City/State/Country
Borgocarbonara Mantova, IT
Establishment Address
VIA UGO RONCADA 83/E, Borgocarbonara Mantova 46020, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GVS SPA (Owner Number: 10094933)
Owner / Operator Contact Address
VIA ROMA 50, Zola Predosa, IT-BO 40069, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPE Container, I.V. General Hospital Class 2 880.5025 2026-01-07
LHI Set, I.V. Fluid Transfer General Hospital Class 2 880.5440 2026-03-24
KPE Container, I.V. General Hospital Class 2 880.5025 2026-03-24

Official Correspondent

Paola Franciosi

US Agent Details

Lorenzo Da Madice Business: ISOPLAN USA Email: isoplan@fda-510k.com Phone: (386) 8680618

Related Public Records

Same Entity

GVS SPA
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9611157 GVS SPA Mirandola Modena, IT

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K041415 B.Braun Medical, Inc. EVA TPN CONTAINER 2004-08-04
K243985 Icu Medical, Inc. Rio™ Drug Reconstitution Transfer Device 2025-01-22
K222718 Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Vial Adapter 2023-03-10

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2020 The Metrix Company 2
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 1500mL, (legless) REF 66615 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Z-0002-2020 The Metrix Company 2
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Z-0003-2020 The Metrix Company 2
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 4000mL, (legless) REF 66640 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Z-0004-2020 The Metrix Company 2
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 1500mL, REF 66616 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Z-0005-2020 The Metrix Company 2
SECURE EVA - DUAL CHAMBER CONTAINER with Manifold, 3000mL, REF 66631 (Canadian distribution) - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9614854. Last updated year: 2026. Please use registration number 9614854 when referencing this establishment in official correspondence.
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