GUDIDData
eudamed_udi Primary ID: D-CNMF000054349DP006GC

BAR Rapid Test Kit(Colloidal gold method) (UDI D-CNMF000054349DP006GC)

Manufactured by Synthgene (Yixing) Health Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BAR Rapid Test Kit(Colloidal gold method) - Primary ID D-CNMF000054349DP006GC

Device Regulatory Overview

The BAR Rapid Test Kit(Colloidal gold method) (Model/Catalog Number: DP006) 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
DP006
Product Code / EMDN
W0102160599
Device Name
BAR Rapid Test Kit(Colloidal gold method)
Database Sync Date
2026-08-09 16:45:58

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of BAR Rapid Test Kit(Colloidal gold method)?

The registered manufacturer of record for BAR Rapid Test Kit(Colloidal gold method) is Synthgene (Yixing) Health Technology Co., Ltd..

What is the Primary UDI-DI identifier for BAR Rapid Test Kit(Colloidal gold method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CNMF000054349DP006GC.

What classification code is assigned to this device?

This device is registered under product classification code W0102160599.

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