GUDIDData
eudamed_udi Primary ID: 08906065481568

Intraveno Safe™ (UDI 08906065481568)

Manufactured by Mais India Medical Devices Pvt. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Intraveno Safe™ - Primary ID 08906065481568

Device Regulatory Overview

The Intraveno Safe™ (Model/Catalog Number: MI/CA/01-000-E) is a medical device manufactured by Mais India Medical Devices Pvt. Ltd.. This product is indexed under FDA Product Code / Category Classification C0101010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MI/CA/01-000-E
Product Code / EMDN
C0101010201
Device Name
IV Cannula/Catheter with Safety Features
Database Sync Date
2026-08-09 16:28:53

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Intraveno Safe™?

The registered manufacturer of record for Intraveno Safe™ is Mais India Medical Devices Pvt. Ltd..

What is the Primary UDI-DI identifier for Intraveno Safe™?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906065481568.

What classification code is assigned to this device?

This device is registered under product classification code C0101010201.

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