eudamed_udi
Primary ID: 04031678093748
Mikrobac forte (UDI 04031678093748)
Manufactured by BODE Chemie GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mikrobac forte - Primary ID 04031678093748
Device Regulatory Overview
The Mikrobac forte (Model/Catalog Number: 982225) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 982225
- Product Code / EMDN
- D99
- Device Name
- Mikrobac
- Database Sync Date
- 2026-08-09 17:37:07
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 Mikrobac forte?
The registered manufacturer of record for Mikrobac forte is BODE Chemie GmbH.
What is the Primary UDI-DI identifier for Mikrobac forte?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678093748.
What classification code is assigned to this device?
This device is registered under product classification code D99.
Similar Classification Devices (D99)
Other Devices by BODE Chemie GmbH
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