gudid
Primary ID: PO2
LEPU MEDICAL (UDI PO2)
Manufactured by Shenzhen Viatom Technology Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LEPU MEDICAL - Primary ID PO2
Device Regulatory Overview
The LEPU MEDICAL (Model/Catalog Number: PO2) is a medical device manufactured by Shenzhen Viatom Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PO2
- Product Code / EMDN
- DQA
- Device Name
- Database Sync Date
- 2026-08-09 09:24:48
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 LEPU MEDICAL?
The registered manufacturer of record for LEPU MEDICAL is Shenzhen Viatom Technology Co.,Ltd..
What is the Primary UDI-DI identifier for LEPU MEDICAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PO2.
What classification code is assigned to this device?
This device is registered under product classification code DQA.
Similar Classification Devices (DQA)
Other Devices by Shenzhen Viatom Technology Co.,Ltd.
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