eudamed_udi
Primary ID: 04031678079735
Bacillol 30 Sensitive Foam (UDI 04031678079735)
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 Foam - Primary ID 04031678079735
Device Regulatory Overview
The Bacillol 30 Sensitive Foam (Model/Catalog Number: 981840) 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
- 981840
- Product Code / EMDN
- D0701
- Device Name
- Bacillol 30 Sensitive
- Database Sync Date
- 2026-08-09 16:30:33
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 30 Sensitive Foam?
The registered manufacturer of record for Bacillol 30 Sensitive Foam is BODE Chemie GmbH.
What is the Primary UDI-DI identifier for Bacillol 30 Sensitive Foam?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678079735.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
Other Devices by BODE Chemie GmbH
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