eudamed_udi
Primary ID: +E25180008851
EC 50 (UDI +E25180008851)
Manufactured by ALPRO MEDICAL GMBH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EC 50 - Primary ID +E25180008851
Device Regulatory Overview
The EC 50 (Model/Catalog Number: 8000885) 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
- 8000885
- Product Code / EMDN
- D99
- Device Name
- BIB forte eco
- Database Sync Date
- 2026-08-09 16:45:51
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 EC 50?
The registered manufacturer of record for EC 50 is ALPRO MEDICAL GMBH.
What is the Primary UDI-DI identifier for EC 50?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +E25180008851.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint