GUDIDData
eudamed_udi Primary ID: 06430080100002

Bacteroides bile esculin (BBE) agarmalja (UDI 06430080100002)

Manufactured by Tammer BioLab Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bacteroides bile esculin (BBE) agarmalja - Primary ID 06430080100002

Device Regulatory Overview

The Bacteroides bile esculin (BBE) agarmalja (Model/Catalog Number: T007) is a medical device manufactured by Tammer BioLab Oy. This product is indexed under FDA Product Code / Category Classification W0104010405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
T007
Product Code / EMDN
W0104010405
Device Name
Bacteroides bile esculin (BBE) agarmalja
Database Sync Date
2026-08-09 16:28:57

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 Bacteroides bile esculin (BBE) agarmalja?

The registered manufacturer of record for Bacteroides bile esculin (BBE) agarmalja is Tammer BioLab Oy.

What is the Primary UDI-DI identifier for Bacteroides bile esculin (BBE) agarmalja?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06430080100002.

What classification code is assigned to this device?

This device is registered under product classification code W0104010405.

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