gudid
Primary ID: 1
STET CUBE (UDI 1)
Manufactured by LIGHT PROGRESS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STET CUBE - Primary ID 1
Device Regulatory Overview
The STET CUBE (Model/Catalog Number: 1) is a medical device manufactured by LIGHT PROGRESS SRL. This product is indexed under FDA Product Code / Category Classification MEC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- MEC
- Device Name
- Database Sync Date
- 2026-08-09 09:04:32
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 STET CUBE?
The registered manufacturer of record for STET CUBE is LIGHT PROGRESS SRL.
What is the Primary UDI-DI identifier for STET CUBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code MEC.
Similar Classification Devices (MEC)
Other Devices by LIGHT PROGRESS SRL
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