GUDIDData
gudid Primary ID: SDKF60101-48T(16*3)

Nucleic Acid Extraction Rapid Kit (Magnetic Bead Method) (UDI SDKF60101-48T(16*3))

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 Nucleic Acid Extraction Rapid Kit (Magnetic Bead Method) - Primary ID SDKF60101-48T(16*3)

Device Regulatory Overview

The Nucleic Acid Extraction Rapid Kit (Magnetic Bead Method) (Model/Catalog Number: SDKF60101-48T(16*3)) 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
SDKF60101-48T(16*3)
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Nucleic Acid Extraction Rapid Kit (Magnetic Bead Method)?

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

What is the Primary UDI-DI identifier for Nucleic Acid Extraction Rapid Kit (Magnetic Bead Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SDKF60101-48T(16*3).

What classification code is assigned to this device?

This device is registered under product classification code JJH.

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