eudamed_udi
Primary ID: 08015662001618
Mobyneb (UDI 08015662001618)
Manufactured by Air Liquide Medical Systems S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mobyneb - Primary ID 08015662001618
Device Regulatory Overview
The Mobyneb (Model/Catalog Number: 400161) is a medical device manufactured by Air Liquide Medical Systems S.r.l.. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 400161
- Product Code / EMDN
- Z12159002
- Device Name
- Mobyneb
- Database Sync Date
- 2026-08-09 16:59:56
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 Mobyneb?
The registered manufacturer of record for Mobyneb is Air Liquide Medical Systems S.r.l..
What is the Primary UDI-DI identifier for Mobyneb?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015662001618.
What classification code is assigned to this device?
This device is registered under product classification code Z12159002.
Similar Classification Devices (Z12159002)
Other Devices by Air Liquide Medical Systems S.r.l.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint