gudid
Primary ID: XM-111
Maynovia (UDI XM-111)
Manufactured by JOYTECH HEALTHCARE CO.,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Maynovia - Primary ID XM-111
Device Regulatory Overview
The Maynovia (Model/Catalog Number: XM-111) is a medical device manufactured by JOYTECH HEALTHCARE CO.,LTD. This product is indexed under FDA Product Code / Category Classification PGJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XM-111
- Product Code / EMDN
- PGJ
- Device Name
- Database Sync Date
- 2026-08-09 09:06:49
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 Maynovia?
The registered manufacturer of record for Maynovia is JOYTECH HEALTHCARE CO.,LTD.
What is the Primary UDI-DI identifier for Maynovia?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XM-111.
What classification code is assigned to this device?
This device is registered under product classification code PGJ.
Similar Classification Devices (PGJ)
Other Devices by JOYTECH HEALTHCARE CO.,LTD
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