GUDIDData
eudamed_udi Primary ID: 08908019743043

DEFIGARD (UDI 08908019743043)

Manufactured by Schiller Healthcare India Pvt Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DEFIGARD - Primary ID 08908019743043

Device Regulatory Overview

The DEFIGARD (Model/Catalog Number: -) is a medical device manufactured by Schiller Healthcare India Pvt Ltd. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
-
Product Code / EMDN
Z12030501
Device Name
DEFIGARD 400x
Database Sync Date
2026-08-09 16:30:00

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 DEFIGARD?

The registered manufacturer of record for DEFIGARD is Schiller Healthcare India Pvt Ltd.

What is the Primary UDI-DI identifier for DEFIGARD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08908019743043.

What classification code is assigned to this device?

This device is registered under product classification code Z12030501.

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