GUDIDData
eudamed_udi Primary ID: 80564505036637

SALMONELLA SELECTIVE SUPPLEMENT VIAL B (UDI 80564505036637)

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 SALMONELLA SELECTIVE SUPPLEMENT VIAL B - Primary ID 80564505036637

Device Regulatory Overview

The SALMONELLA SELECTIVE SUPPLEMENT VIAL B (Model/Catalog Number: 4240013B) is a medical device manufactured by Biolife Italiana s.r.l.. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
4240013B
Product Code / EMDN
W0104010104
Device Name
ADDITIVES FOR CULTURE MEDIA
Database Sync Date
2026-08-09 17:25:04

Full Regulatory Attributes

πŸ”’ 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 SALMONELLA SELECTIVE SUPPLEMENT VIAL B?

The registered manufacturer of record for SALMONELLA SELECTIVE SUPPLEMENT VIAL B is Biolife Italiana s.r.l..

What is the Primary UDI-DI identifier for SALMONELLA SELECTIVE SUPPLEMENT VIAL B?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 80564505036637.

What classification code is assigned to this device?

This device is registered under product classification code W0104010104.

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