gudid
Primary ID: 20902504
Perseus (UDI 20902504)
Manufactured by ORTHOKEY ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Perseus - Primary ID 20902504
Device Regulatory Overview
The Perseus (Model/Catalog Number: 20902504) is a medical device manufactured by ORTHOKEY ITALIA SRL. This product is indexed under FDA Product Code / Category Classification OLO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20902504
- Product Code / EMDN
- OLO
- Device Name
- Perseus Tibial Cutting Guide R - 1.3 mm
- Database Sync Date
- 2026-08-09 09:04:32
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 Perseus?
The registered manufacturer of record for Perseus is ORTHOKEY ITALIA SRL.
What is the Primary UDI-DI identifier for Perseus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 20902504.
What classification code is assigned to this device?
This device is registered under product classification code OLO.
Similar Classification Devices (OLO)
Other Devices by ORTHOKEY ITALIA SRL
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint