SDJMASTERVISION (UDI MVD01)
Manufactured by Tianjin Mastervision Technology Co., Ltd.
Device Regulatory Overview
The SDJMASTERVISION (Model/Catalog Number: MVD01) is a medical device manufactured by Tianjin Mastervision Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MVD01
- Product Code / EMDN
- HQD
- Device Name
- Database Sync Date
- 2026-08-09 09:06:36
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 SDJMASTERVISION?
The registered manufacturer of record for SDJMASTERVISION is Tianjin Mastervision Technology Co., Ltd..
What is the Primary UDI-DI identifier for SDJMASTERVISION?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MVD01.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by Tianjin Mastervision Technology Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint