GUDIDData
gudid Primary ID: 2 ways

SET GRI-FILL 3.0 (UDI 2 ways)

Manufactured by LABORATORIOS GRIFOLS SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SET GRI-FILL 3.0 - Primary ID 2 ways

Device Regulatory Overview

The SET GRI-FILL 3.0 (Model/Catalog Number: 2 ways) is a medical device manufactured by LABORATORIOS GRIFOLS SA. This product is indexed under FDA Product Code / Category Classification LHI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2 ways
Product Code / EMDN
LHI
Device Name
SETS GRI-FILL 3.0 are fluid transfer sets for use with the GRI-FILL 3.0 pharmacy compounding device in order to compound or mix different multi-ingredient solutions and to channel them into a final suitable IV container. The set is a disposable component of the compounding device. The 1 WAY / 2 WAY models are made up of a syringe, a distributor, tubing to channel the fluid and a waste/residue bag. Sets are available for 1 or 2 source substances. Also a Luer female - female adapter is available as an accessory to the 1 or 2 way transfer sets. The MULTIPLE model is also used as an accessory with the 1IWAY I 2WAY sets for channeling the same solution from up to six (6) source containers delivering them into a final IV container. It is made up of connectors and tubing to enable interconnection of the different source containers.
Database Sync Date
2026-08-09 09:10:50

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SET GRI-FILL 3.0?

The registered manufacturer of record for SET GRI-FILL 3.0 is LABORATORIOS GRIFOLS SA.

What is the Primary UDI-DI identifier for SET GRI-FILL 3.0?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2 ways.

What classification code is assigned to this device?

This device is registered under product classification code LHI.

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