GUDIDData
eudamed_udi Primary ID: 05902643925588

Legionella CYE Supplement with Cysteine (UDI 05902643925588)

Manufactured by BioMaxima Spółka Akcyjna

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Legionella CYE Supplement with Cysteine - Primary ID 05902643925588

Device Regulatory Overview

The Legionella CYE Supplement with Cysteine (Model/Catalog Number: SL 0053) is a medical device manufactured by BioMaxima Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SL 0053
Product Code / EMDN
W0104010104
Device Name
Legionella CYE Growth Supplement
Database Sync Date
2026-08-09 16:58:38

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 Legionella CYE Supplement with Cysteine?

The registered manufacturer of record for Legionella CYE Supplement with Cysteine is BioMaxima Spółka Akcyjna.

What is the Primary UDI-DI identifier for Legionella CYE Supplement with Cysteine?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643925588.

What classification code is assigned to this device?

This device is registered under product classification code W0104010104.

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