Unspecified Brand (UDI 07502273992325)
Manufactured by Oculus Technologies of México S.A. de C.V.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: P-E392T00) 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 Q02030299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P-E392T00
- Product Code / EMDN
- Q02030299
- Device Name
- Ocudox
- Database Sync Date
- 2026-08-09 16:29:13
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Oculus Technologies of México S.A. de C.V..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07502273992325.
What classification code is assigned to this device?
This device is registered under product classification code Q02030299.
Similar Classification Devices (Q02030299)
Other Devices by Oculus Technologies of México S.A. de C.V.
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