eudamed_udi Primary ID: 04260760134797

Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK)) (UDI 04260760134797)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK)) (Model/Catalog Number: S009.02.) is a medical device manufactured by Solabia Xebios GmbH. This product is indexed under FDA Product Code / Category Classification W0104030201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S009.02.
Product Code / EMDN: W0104030201
Device Name: Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK))
Database Sync Date: 2026-08-09 16:30:24

Full Regulatory Attributes

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{
    "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 Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK))?

The registered manufacturer of record for Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK)) is Solabia Xebios GmbH.

What is the Primary UDI-DI identifier for Sab Dextr Agar mod. (Takashio's Agar) (SAB DEX M (TAK))?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260760134797.

What classification code is assigned to this device?

This device is registered under product classification code W0104030201.

Similar Classification Devices (W0104030201)

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