GUDIDData
eudamed_udi Primary ID: 08015662723978

INEVA N1 Silent (UDI 08015662723978)

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 INEVA N1 Silent - Primary ID 08015662723978

Device Regulatory Overview

The INEVA N1 Silent (Model/Catalog Number: 472397) is a medical device manufactured by Air Liquide Medical Systems S.r.l.. This product is indexed under FDA Product Code / Category Classification R0301010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
472397
Product Code / EMDN
R0301010201
Device Name
INEVA N1 Silent
Database Sync Date
2026-08-09 16:30:06

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 INEVA N1 Silent?

The registered manufacturer of record for INEVA N1 Silent is Air Liquide Medical Systems S.r.l..

What is the Primary UDI-DI identifier for INEVA N1 Silent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015662723978.

What classification code is assigned to this device?

This device is registered under product classification code R0301010201.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint