eudamed_udi
Primary ID: 05907514612123
Liquick Cor-ALP 60 (UDI 05907514612123)
Manufactured by PZ CORMAY Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Liquick Cor-ALP 60 - Primary ID 05907514612123
Device Regulatory Overview
The Liquick Cor-ALP 60 (Model/Catalog Number: 1-212) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1-212
- Product Code / EMDN
- W01010105
- Device Name
- ALP
- Database Sync Date
- 2026-08-09 17:17:23
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 Liquick Cor-ALP 60?
The registered manufacturer of record for Liquick Cor-ALP 60 is PZ CORMAY Spółka Akcyjna.
What is the Primary UDI-DI identifier for Liquick Cor-ALP 60?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514612123.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by PZ CORMAY Spółka Akcyjna
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint