GUDIDData
gudid Primary ID: MULTIPLE

FLEBOSET (UDI MULTIPLE)

Manufactured by LABORATORIOS GRIFOLS SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLEBOSET - Primary ID MULTIPLE

Device Regulatory Overview

The FLEBOSET (Model/Catalog Number: MULTIPLE) 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
MULTIPLE
Product Code / EMDN
LHI
Device Name
FLEBOSET MULTIPLE is a fluid transfer tubing set used to enable continuous (uninterrupted) delivery of drug solutions from 6 glass source containers. It is used in pharmacy compounding or for IV fluid transfer to minimize manipulation when working with small volumen source containers. The device is made up of 6 spikes connected in series with flexible tubing segments, each segment with an idividual clamp. The set terminal, for connection to the pharmacy compounding device sets or administration sets (gravity or pump) consists of a spikeable twist-off valve connector.
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 FLEBOSET?

The registered manufacturer of record for FLEBOSET is LABORATORIOS GRIFOLS SA.

What is the Primary UDI-DI identifier for FLEBOSET?

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

What classification code is assigned to this device?

This device is registered under product classification code LHI.

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