GUDIDData
eudamed_udi Primary ID: 00860004068808

Broncholab (UDI 00860004068808)

Manufactured by FLUIDDA NV

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Broncholab - Primary ID 00860004068808

Device Regulatory Overview

The Broncholab (Model/Catalog Number: 1.1.1) is a medical device manufactured by FLUIDDA NV. This product is indexed under FDA Product Code / Category Classification Z12159082 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1.1.1
Product Code / EMDN
Z12159082
Device Name
Broncholab
Database Sync Date
2026-08-09 16:46:02

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 Broncholab?

The registered manufacturer of record for Broncholab is FLUIDDA NV.

What is the Primary UDI-DI identifier for Broncholab?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00860004068808.

What classification code is assigned to this device?

This device is registered under product classification code Z12159082.

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