GUDIDData
eudamed_udi Primary ID: 06931038660024

Electronic sphygmomanometer (UDI 06931038660024)

Manufactured by Wenzhou Bokang Instruments Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Electronic sphygmomanometer - Primary ID 06931038660024

Device Regulatory Overview

The Electronic sphygmomanometer (Model/Catalog Number: BK6002) is a medical device manufactured by Wenzhou Bokang Instruments Co.,Ltd. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BK6002
Product Code / EMDN
C9006
Device Name
Electronic sphygmomanometer
Database Sync Date
2026-08-09 17:21:42

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 Electronic sphygmomanometer?

The registered manufacturer of record for Electronic sphygmomanometer is Wenzhou Bokang Instruments Co.,Ltd.

What is the Primary UDI-DI identifier for Electronic sphygmomanometer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931038660024.

What classification code is assigned to this device?

This device is registered under product classification code C9006.

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