GUDIDData
eudamed_udi Primary ID: 05940540372258

AGAR PYKOVSKAIA (PIKOVSKAYA'S AGAR) (UDI 05940540372258)

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 PYKOVSKAIA (PIKOVSKAYA'S AGAR) - Primary ID 05940540372258

Device Regulatory Overview

The AGAR PYKOVSKAIA (PIKOVSKAYA'S AGAR) (Model/Catalog Number: 400195) is a medical device manufactured by Sanimed International Impex S.A.. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
400195
Product Code / EMDN
W0104010101
Device Name
AGAR PYKOVSKAIA (PIKOVSKAYA'S AGAR)
Database Sync Date
2026-08-09 16:47:30

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 PYKOVSKAIA (PIKOVSKAYA'S AGAR)?

The registered manufacturer of record for AGAR PYKOVSKAIA (PIKOVSKAYA'S AGAR) is Sanimed International Impex S.A..

What is the Primary UDI-DI identifier for AGAR PYKOVSKAIA (PIKOVSKAYA'S AGAR)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05940540372258.

What classification code is assigned to this device?

This device is registered under product classification code W0104010101.

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