GUDIDData
eudamed_udi Primary ID: 06973315739368

Vazyme Target Capture Hybridization and Wash Pro Kit (UDI 06973315739368)

Manufactured by Nanjing Vazyme Medical Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vazyme Target Capture Hybridization and Wash Pro Kit - Primary ID 06973315739368

Device Regulatory Overview

The Vazyme Target Capture Hybridization and Wash Pro Kit (Model/Catalog Number: NC401ME-C1-P1) is a medical device manufactured by Nanjing Vazyme Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W010699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
NC401ME-C1-P1
Product Code / EMDN
W010699
Device Name
Vazyme Target Capture Hybridization and Wash Pro Kit
Database Sync Date
2026-08-09 16:48:58

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 Vazyme Target Capture Hybridization and Wash Pro Kit?

The registered manufacturer of record for Vazyme Target Capture Hybridization and Wash Pro Kit is Nanjing Vazyme Medical Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Vazyme Target Capture Hybridization and Wash Pro Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973315739368.

What classification code is assigned to this device?

This device is registered under product classification code W010699.

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