eudamed_udi
Primary ID: 05907514644902
PRESTIGE 24i LDL DIRECT (UDI 05907514644902)
Manufactured by PZ CORMAY Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRESTIGE 24i LDL DIRECT - Primary ID 05907514644902
Device Regulatory Overview
The PRESTIGE 24i LDL DIRECT (Model/Catalog Number: 4-490) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4-490
- Product Code / EMDN
- W01010221
- Device Name
- LDL DIRECT
- Database Sync Date
- 2026-08-09 17:59:34
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 PRESTIGE 24i LDL DIRECT?
The registered manufacturer of record for PRESTIGE 24i LDL DIRECT is PZ CORMAY Spółka Akcyjna.
What is the Primary UDI-DI identifier for PRESTIGE 24i LDL DIRECT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514644902.
What classification code is assigned to this device?
This device is registered under product classification code W01010221.
Similar Classification Devices (W01010221)
Other Devices by PZ CORMAY Spółka Akcyjna
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