eudamed_udi
Primary ID: +E2512237481
KDM Biodes-K Forte Eco (UDI +E2512237481)
Manufactured by ALPRO MEDICAL GMBH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KDM Biodes-K Forte Eco - Primary ID +E2512237481
Device Regulatory Overview
The KDM Biodes-K Forte Eco (Model/Catalog Number: 223748) is a medical device manufactured by ALPRO MEDICAL GMBH. This product is indexed under FDA Product Code / Category Classification D99 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 223748
- Product Code / EMDN
- D99
- Device Name
- BIB forte eco
- Database Sync Date
- 2026-08-09 16:29:15
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 KDM Biodes-K Forte Eco?
The registered manufacturer of record for KDM Biodes-K Forte Eco is ALPRO MEDICAL GMBH.
What is the Primary UDI-DI identifier for KDM Biodes-K Forte Eco?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E2512237481.
What classification code is assigned to this device?
This device is registered under product classification code D99.
Similar Classification Devices (D99)
Other Devices by ALPRO MEDICAL GMBH
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