gudid
Primary ID: SL-FR02S
VU (UDI SL-FR02S)
Manufactured by Xiamen Weiyou Intelligent Technology Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VU - Primary ID SL-FR02S
Device Regulatory Overview
The VU (Model/Catalog Number: SL-FR02S) is a medical device manufactured by Xiamen Weiyou Intelligent Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification ISA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SL-FR02S
- Product Code / EMDN
- ISA
- Device Name
- hand rehabilitation robot
- Database Sync Date
- 2026-08-09 09:06:44
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 VU?
The registered manufacturer of record for VU is Xiamen Weiyou Intelligent Technology Co.,Ltd.
What is the Primary UDI-DI identifier for VU?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SL-FR02S.
What classification code is assigned to this device?
This device is registered under product classification code ISA.
Similar Classification Devices (ISA)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint