eudamed_udi
Primary ID: 05710188020770
CryoPro Liquid Nitrogen Filter (UDI 05710188020770)
Manufactured by Cortex Technology Aps
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CryoPro Liquid Nitrogen Filter - Primary ID 05710188020770
Device Regulatory Overview
The CryoPro Liquid Nitrogen Filter (Model/Catalog Number: LNF) is a medical device manufactured by Cortex Technology Aps. This product is indexed under FDA Product Code / Category Classification Z120102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LNF
- Product Code / EMDN
- Z120102
- Device Name
- CryoPro Liquid Nitrogen Filter
- Database Sync Date
- 2026-08-09 17:38:15
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 CryoPro Liquid Nitrogen Filter?
The registered manufacturer of record for CryoPro Liquid Nitrogen Filter is Cortex Technology Aps.
What is the Primary UDI-DI identifier for CryoPro Liquid Nitrogen Filter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05710188020770.
What classification code is assigned to this device?
This device is registered under product classification code Z120102.
Similar Classification Devices (Z120102)
Other Devices by Cortex Technology Aps
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint