eudamed_udi
Primary ID: 08015662011624
Nebula (UDI 08015662011624)
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 Nebula - Primary ID 08015662011624
Device Regulatory Overview
The Nebula (Model/Catalog Number: 401162) 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
- 401162
- Product Code / EMDN
- Z12159002
- Device Name
- Nebula
- Database Sync Date
- 2026-08-09 16:30:03
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Nebula?
The registered manufacturer of record for Nebula is Air Liquide Medical Systems S.r.l..
What is the Primary UDI-DI identifier for Nebula?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015662011624.
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.
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