GUDIDData
gudid Primary ID: 48 Tests

Bacteria DNA Extraction Kit (Magnetic Bead Method) (UDI 48 Tests)

Manufactured by Jiangsu Bioperfectus Technologies Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bacteria DNA Extraction Kit (Magnetic Bead Method) - Primary ID 48 Tests

Device Regulatory Overview

The Bacteria DNA Extraction Kit (Magnetic Bead Method) (Model/Catalog Number: 48 Tests) is a medical device manufactured by Jiangsu Bioperfectus Technologies Co., Ltd.. This product is indexed under FDA Product Code / Category Classification JJH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
48 Tests
Product Code / EMDN
JJH
Device Name
Database Sync Date
2026-08-09 09:06:39

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 Bacteria DNA Extraction Kit (Magnetic Bead Method)?

The registered manufacturer of record for Bacteria DNA Extraction Kit (Magnetic Bead Method) is Jiangsu Bioperfectus Technologies Co., Ltd..

What is the Primary UDI-DI identifier for Bacteria DNA Extraction Kit (Magnetic Bead Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48 Tests.

What classification code is assigned to this device?

This device is registered under product classification code JJH.

Programmatic Export

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

JSON API Endpoint