GUDIDData
eudamed_udi Primary ID: 06959352702190

Sleep Apnoea Therapy Devices (UDI 06959352702190)

Manufactured by Micomme Medical Technology Development Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sleep Apnoea Therapy Devices - Primary ID 06959352702190

Device Regulatory Overview

The Sleep Apnoea Therapy Devices (Model/Catalog Number: /) is a medical device manufactured by Micomme Medical Technology Development Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q03010299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
/
Product Code / EMDN
Q03010299
Device Name
Sleep Apnoea Therapy Devices
Database Sync Date
2026-08-09 17:43:38

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 Therapy Devices?

The registered manufacturer of record for Sleep Apnoea Therapy Devices is Micomme Medical Technology Development Co., Ltd..

What is the Primary UDI-DI identifier for Sleep Apnoea Therapy Devices?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06959352702190.

What classification code is assigned to this device?

This device is registered under product classification code Q03010299.

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