GUDIDData
eudamed_udi Primary ID: 08054187132285

xld agar (UDI 08054187132285)

Manufactured by Biolife Italiana s.r.l.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for xld agar - Primary ID 08054187132285

Device Regulatory Overview

The xld agar (Model/Catalog Number: 542206) is a medical device manufactured by Biolife Italiana s.r.l.. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
542206
Product Code / EMDN
W0104010405
Device Name
MEDIAPLATES
Database Sync Date
2026-08-09 16:29:02

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 xld agar?

The registered manufacturer of record for xld agar is Biolife Italiana s.r.l..

What is the Primary UDI-DI identifier for xld agar?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08054187132285.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

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