eudamed_udi
Primary ID: 04270001023551
Asthma Optimiser (UDI 04270001023551)
Manufactured by Lothar Medtec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Asthma Optimiser - Primary ID 04270001023551
Device Regulatory Overview
The Asthma Optimiser (Model/Catalog Number: Asthma Optimiser) is a medical device manufactured by Lothar Medtec GmbH. This product is indexed under FDA Product Code / Category Classification Z12159092 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Asthma Optimiser
- Product Code / EMDN
- Z12159092
- Device Name
- Treatment Optimiser
- Database Sync Date
- 2026-08-09 18:08:05
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Asthma Optimiser?
The registered manufacturer of record for Asthma Optimiser is Lothar Medtec GmbH.
What is the Primary UDI-DI identifier for Asthma Optimiser?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04270001023551.
What classification code is assigned to this device?
This device is registered under product classification code Z12159092.
Similar Classification Devices (Z12159092)
Other Devices by Lothar Medtec GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint