GUDIDData
eudamed_udi Primary ID: 08906030753409

Meditor (UDI 08906030753409)

Manufactured by Lars Medicare Pvt Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Meditor - Primary ID 08906030753409

Device Regulatory Overview

The Meditor (Model/Catalog Number: 294 - 1036.26) is a medical device manufactured by Lars Medicare Pvt Ltd. This product is indexed under FDA Product Code / Category Classification C0101010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
294 - 1036.26
Product Code / EMDN
C0101010101
Device Name
I.V cannula
Database Sync Date
2026-08-09 16:28:49

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 Meditor?

The registered manufacturer of record for Meditor is Lars Medicare Pvt Ltd.

What is the Primary UDI-DI identifier for Meditor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906030753409.

What classification code is assigned to this device?

This device is registered under product classification code C0101010101.

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