GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 06955931302874

Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis) (UDI 06955931302874)

Manufactured by Yaneng BIOscience (Shenzhen) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis) - Primary ID 06955931302874

Device Regulatory Overview

The Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis) (Model/Catalog Number: 212901) is a medical device manufactured by Yaneng BIOscience (Shenzhen) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0105041005 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
212901
Product Code / EMDN
W0105041005
Device Name
Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis)
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 Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis)?

The registered manufacturer of record for Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis) is Yaneng BIOscience (Shenzhen) Co., Ltd..

What is the Primary UDI-DI identifier for Human Papillomavirus Genotyping Kit (Multicolor Melting Curve Analysis)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06955931302874.

What classification code is assigned to this device?

This device is registered under product classification code W0105041005.

Similar Classification Devices (W0105041005)

Other Devices by Yaneng BIOscience (Shenzhen) Co., Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint