eudamed_udi
Primary ID: 04031678057573
Korsolex PAA (UDI 04031678057573)
Manufactured by BODE Chemie GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Korsolex PAA - Primary ID 04031678057573
Device Regulatory Overview
The Korsolex PAA (Model/Catalog Number: 981210) is a medical device manufactured by BODE Chemie GmbH. This product is indexed under FDA Product Code / Category Classification D050103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 981210
- Product Code / EMDN
- D050103
- Device Name
- Korsolex PAA
- Database Sync Date
- 2026-08-09 18:38:59
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Korsolex PAA?
The registered manufacturer of record for Korsolex PAA is BODE Chemie GmbH.
What is the Primary UDI-DI identifier for Korsolex PAA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04031678057573.
What classification code is assigned to this device?
This device is registered under product classification code D050103.
Similar Classification Devices (D050103)
Other Devices by BODE Chemie GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint