GUDIDData
eudamed_udi Primary ID: 07640156398472

MED-130 Compressor nebulizer (UDI 07640156398472)

Manufactured by B.Well Swiss AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MED-130 Compressor nebulizer - Primary ID 07640156398472

Device Regulatory Overview

The MED-130 Compressor nebulizer (Model/Catalog Number: 1101596) is a medical device manufactured by B.Well Swiss AG. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1101596
Product Code / EMDN
Z12159002
Device Name
Compressor nebulizer
Database Sync Date
2026-08-09 18:39:40

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 MED-130 Compressor nebulizer?

The registered manufacturer of record for MED-130 Compressor nebulizer is B.Well Swiss AG.

What is the Primary UDI-DI identifier for MED-130 Compressor nebulizer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07640156398472.

What classification code is assigned to this device?

This device is registered under product classification code Z12159002.

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