Electromicyn60 (UDI 07502273999935)
Manufactured by Oculus Technologies of México S.A. de C.V.
Device Regulatory Overview
The Electromicyn60 (Model/Catalog Number: P-E1376T00) 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 D03010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- P-E1376T00
- Product Code / EMDN
- D03010101
- Device Name
- Microsafe
- Database Sync Date
- 2026-08-09 16:30:03
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 Electromicyn60?
The registered manufacturer of record for Electromicyn60 is Oculus Technologies of México S.A. de C.V..
What is the Primary UDI-DI identifier for Electromicyn60?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07502273999935.
What classification code is assigned to this device?
This device is registered under product classification code D03010101.
Similar Classification Devices (D03010101)
Other Devices by Oculus Technologies of México S.A. de C.V.
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