GUDIDData
eudamed_udi Primary ID: 06946725503836

Blood pressure cuff (UDI 06946725503836)

Manufactured by APK Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Blood pressure cuff - Primary ID 06946725503836

Device Regulatory Overview

The Blood pressure cuff (Model/Catalog Number: A-XT-04D(4)-U3) is a medical device manufactured by APK Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z1203020599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A-XT-04D(4)-U3
Product Code / EMDN
Z1203020599
Device Name
Blood pressure cuff
Database Sync Date
2026-08-09 16:29:47

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 Blood pressure cuff?

The registered manufacturer of record for Blood pressure cuff is APK Technology Co., Ltd..

What is the Primary UDI-DI identifier for Blood pressure cuff?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06946725503836.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020599.

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