eudamed_udi
Primary ID: 03700504302170
MONNAL TEO (UDI 03700504302170)
Manufactured by Air Liquide Medical Systems S.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MONNAL TEO - Primary ID 03700504302170
Device Regulatory Overview
The MONNAL TEO (Model/Catalog Number: KB040019) is a medical device manufactured by Air Liquide Medical Systems S.A.. This product is indexed under FDA Product Code / Category Classification Z1203010504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KB040019
- Product Code / EMDN
- Z1203010504
- Device Name
- MONNAL TEO
- Database Sync Date
- 2026-08-09 16:29:31
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 MONNAL TEO?
The registered manufacturer of record for MONNAL TEO is Air Liquide Medical Systems S.A..
What is the Primary UDI-DI identifier for MONNAL TEO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03700504302170.
What classification code is assigned to this device?
This device is registered under product classification code Z1203010504.
Similar Classification Devices (Z1203010504)
Other Devices by Air Liquide Medical Systems S.A.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint