ALVEA (UDI 08050713840419)
Manufactured by Air Liquide Italia Gas e Servizi S.r.l.
Device Regulatory Overview
The ALVEA (Model/Catalog Number: FT21ALVEA00000) is a medical device manufactured by Air Liquide Italia Gas e Servizi S.r.l.. This product is indexed under FDA Product Code / Category Classification Z120309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FT21ALVEA00000
- Product Code / EMDN
- Z120309
- Device Name
- CARRELLO DI EMERGENZA PER IMPIANTO DI DISTRIBUZIONE GAS MEDICINALI ALVEA
- Database Sync Date
- 2026-08-09 18:57:18
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 ALVEA?
The registered manufacturer of record for ALVEA is Air Liquide Italia Gas e Servizi S.r.l..
What is the Primary UDI-DI identifier for ALVEA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050713840419.
What classification code is assigned to this device?
This device is registered under product classification code Z120309.
Similar Classification Devices (Z120309)
Other Devices by Air Liquide Italia Gas e Servizi S.r.l.
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