eudamed_udi
Primary ID: 05204309173716
LDH L-P (UDI 05204309173716)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LDH L-P - Primary ID 05204309173716
Device Regulatory Overview
The LDH L-P (Model/Catalog Number: 1415-0112) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W01010119 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1415-0112
- Product Code / EMDN
- W01010119
- Device Name
- LDH L-P
- Database Sync Date
- 2026-08-09 16:48:13
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 LDH L-P?
The registered manufacturer of record for LDH L-P is Medicon Hellas SA.
What is the Primary UDI-DI identifier for LDH L-P?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309173716.
What classification code is assigned to this device?
This device is registered under product classification code W01010119.
Similar Classification Devices (W01010119)
Other Devices by Medicon Hellas SA
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