GUDIDData
eudamed_udi Primary ID: 05940540375105

AGAR NITRAT (NITRATE AGAR) (UDI 05940540375105)

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 AGAR NITRAT (NITRATE AGAR) - Primary ID 05940540375105

Device Regulatory Overview

The AGAR NITRAT (NITRATE AGAR) (Model/Catalog Number: 30381) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010206 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
30381
Product Code / EMDN
W0104010206
Device Name
AGAR NITRAT (NITRATE AGAR)
Database Sync Date
2026-08-09 16:29:56

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 AGAR NITRAT (NITRATE AGAR)?

The registered manufacturer of record for AGAR NITRAT (NITRATE AGAR) is Sanimed International Impex S.A..

What is the Primary UDI-DI identifier for AGAR NITRAT (NITRATE AGAR)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540375105.

What classification code is assigned to this device?

This device is registered under product classification code W0104010206.

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