eudamed_udi
Primary ID: 04031678093083
Kohrsolin FF (UDI 04031678093083)
Manufactured by BODE Chemie GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kohrsolin FF - Primary ID 04031678093083
Device Regulatory Overview
The Kohrsolin FF (Model/Catalog Number: 982190) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 982190
- Product Code / EMDN
- D01010101
- Device Name
- Kohrsolin
- Database Sync Date
- 2026-08-09 18:26:02
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 Kohrsolin FF?
The registered manufacturer of record for Kohrsolin FF is BODE Chemie GmbH.
What is the Primary UDI-DI identifier for Kohrsolin FF?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678093083.
What classification code is assigned to this device?
This device is registered under product classification code D01010101.
Similar Classification Devices (D01010101)
Other Devices by BODE Chemie GmbH
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