Unspecified Brand (UDI 08050713840013)
Manufactured by Air Liquide Italia Gas e Servizi S.r.l.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: M5120M14R0A001) 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 V9099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M5120M14R0A001
- Product Code / EMDN
- V9099
- Device Name
- CO2 D.M. COLTURA CELLULARE Bombola 14 Litri Valv. REGULAR
- Database Sync Date
- 2026-08-09 16:44:53
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Air Liquide Italia Gas e Servizi S.r.l..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050713840013.
What classification code is assigned to this device?
This device is registered under product classification code V9099.
Similar Classification Devices (V9099)
Other Devices by Air Liquide Italia Gas e Servizi S.r.l.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint