GUDIDData
eudamed_udi Primary ID: 06972955510061

Sleep Apnoea Breathing Therapy Devices(BiPAP Devices) (UDI 06972955510061)

Manufactured by Shenzhen Yamind Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sleep Apnoea Breathing Therapy Devices(BiPAP Devices) - Primary ID 06972955510061

Device Regulatory Overview

The Sleep Apnoea Breathing Therapy Devices(BiPAP Devices) (Model/Catalog Number: 6632) is a medical device manufactured by Shenzhen Yamind Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12030102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6632
Product Code / EMDN
Z12030102
Device Name
Sleep Apnoea Breathing Therapy Devices(BiPAP Devices)
Database Sync Date
2026-08-09 16:46:47

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 Sleep Apnoea Breathing Therapy Devices(BiPAP Devices)?

The registered manufacturer of record for Sleep Apnoea Breathing Therapy Devices(BiPAP Devices) is Shenzhen Yamind Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Sleep Apnoea Breathing Therapy Devices(BiPAP Devices)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972955510061.

What classification code is assigned to this device?

This device is registered under product classification code Z12030102.

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