eudamed_udi
Primary ID: 04031678035328
Bacillol AF (UDI 04031678035328)
Manufactured by BODE Chemie GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bacillol AF - Primary ID 04031678035328
Device Regulatory Overview
The Bacillol AF (Model/Catalog Number: 975170) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D0799 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 975170
- Product Code / EMDN
- D0799
- Device Name
- Bacillol AF
- Database Sync Date
- 2026-08-09 16:44:53
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Bacillol AF?
The registered manufacturer of record for Bacillol AF is BODE Chemie GmbH.
What is the Primary UDI-DI identifier for Bacillol AF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678035328.
What classification code is assigned to this device?
This device is registered under product classification code D0799.
Similar Classification Devices (D0799)
Other Devices by BODE Chemie GmbH
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