GUDIDData
eudamed_udi Primary ID: 04031678079902

Bacillol 30 Sensitive Tissues (UDI 04031678079902)

Manufactured by BODE Chemie GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bacillol 30 Sensitive Tissues - Primary ID 04031678079902

Device Regulatory Overview

The Bacillol 30 Sensitive Tissues (Model/Catalog Number: 981848) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
981848
Product Code / EMDN
D0701
Device Name
Bacillol 30 Sensitive
Database Sync Date
2026-08-09 18:01:23

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 Bacillol 30 Sensitive Tissues?

The registered manufacturer of record for Bacillol 30 Sensitive Tissues is BODE Chemie GmbH.

What is the Primary UDI-DI identifier for Bacillol 30 Sensitive Tissues?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678079902.

What classification code is assigned to this device?

This device is registered under product classification code D0701.

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