GUDIDData
eudamed_udi Primary ID: 05940540371114

CLORURA FERICA 10% (UDI 05940540371114)

Manufactured by Sanimed International Impex S.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CLORURA FERICA 10% - Primary ID 05940540371114

Device Regulatory Overview

The CLORURA FERICA 10% (Model/Catalog Number: 13040) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010306 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
13040
Product Code / EMDN
W0104010306
Device Name
CLORURA FERICA 10%
Database Sync Date
2026-08-09 16:48:01

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 CLORURA FERICA 10%?

The registered manufacturer of record for CLORURA FERICA 10% is Sanimed International Impex S.A..

What is the Primary UDI-DI identifier for CLORURA FERICA 10%?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540371114.

What classification code is assigned to this device?

This device is registered under product classification code W0104010306.

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