GUDIDData
eudamed_udi Primary ID: 05902643925113

Campylobacter Selective Supplement Skirrow (UDI 05902643925113)

Manufactured by BioMaxima Spółka Akcyjna

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Campylobacter Selective Supplement Skirrow - Primary ID 05902643925113

Device Regulatory Overview

The Campylobacter Selective Supplement Skirrow (Model/Catalog Number: SL 0006) 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 0006
Product Code / EMDN
W0104010104
Device Name
Campylobacter CCDA Selective Supplement
Database Sync Date
2026-08-09 17:30:03

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 Campylobacter Selective Supplement Skirrow?

The registered manufacturer of record for Campylobacter Selective Supplement Skirrow is BioMaxima Spółka Akcyjna.

What is the Primary UDI-DI identifier for Campylobacter Selective Supplement Skirrow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643925113.

What classification code is assigned to this device?

This device is registered under product classification code W0104010104.

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