gudid
Primary ID: ODOA-856EUO
T-Cube (UDI ODOA-856EUO)
Manufactured by WONDFO USA CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for T-Cube - Primary ID ODOA-856EUO
Device Regulatory Overview
The T-Cube (Model/Catalog Number: ODOA-856EUO) is a medical device manufactured by WONDFO USA CO., LTD.. This product is indexed under FDA Product Code / Category Classification LCM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ODOA-856EUO
- Product Code / EMDN
- LCM
- Device Name
- 5-Panel T-Cube; AMP,COC,MET,OPI,PCP
- Database Sync Date
- 2026-08-09 09:31:26
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 T-Cube?
The registered manufacturer of record for T-Cube is WONDFO USA CO., LTD..
What is the Primary UDI-DI identifier for T-Cube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ODOA-856EUO.
What classification code is assigned to this device?
This device is registered under product classification code LCM.
Similar Classification Devices (LCM)
Other Devices by WONDFO USA CO., LTD.
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