MDPV Rapid Test Kit (Colloidal gold method) (UDI D-CNMF000054349DP030G9)
Manufactured by Synthgene (Yixing) Health Technology Co., Ltd.
Device Regulatory Overview
The MDPV Rapid Test Kit (Colloidal gold method) (Model/Catalog Number: DP030) is a medical device manufactured by Synthgene (Yixing) Health Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DP030
- Product Code / EMDN
- W0102160599
- Device Name
- MDPV Rapid Test Kit (Colloidal gold method)
- Database Sync Date
- 2026-08-09 16:29:05
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 MDPV Rapid Test Kit (Colloidal gold method)?
The registered manufacturer of record for MDPV Rapid Test Kit (Colloidal gold method) is Synthgene (Yixing) Health Technology Co., Ltd..
What is the Primary UDI-DI identifier for MDPV Rapid Test Kit (Colloidal gold method)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CNMF000054349DP030G9.
What classification code is assigned to this device?
This device is registered under product classification code W0102160599.
Similar Classification Devices (W0102160599)
Other Devices by Synthgene (Yixing) Health Technology Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint