Microdacyn60 (UDI 07502273992332)
Manufactured by Oculus Technologies of México S.A. de C.V.
Device Regulatory Overview
The Microdacyn60 (Model/Catalog Number: P-E393T00) is a medical device manufactured by Oculus Technologies of México S.A. de C.V.. This product is indexed under FDA Product Code / Category Classification M040499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P-E393T00
- Product Code / EMDN
- M040499
- Device Name
- Microdacyn60 Wound Care
- Database Sync Date
- 2026-08-09 16:45:03
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 Microdacyn60?
The registered manufacturer of record for Microdacyn60 is Oculus Technologies of México S.A. de C.V..
What is the Primary UDI-DI identifier for Microdacyn60?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07502273992332.
What classification code is assigned to this device?
This device is registered under product classification code M040499.
Similar Classification Devices (M040499)
Other Devices by Oculus Technologies of México S.A. de C.V.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint