GUDIDData
eudamed_udi Primary ID: D-MYO706-AED7

MYO Myoglobin (CLIA) (UDI D-MYO706-AED7)

Manufactured by Hangzhou Aichek Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MYO Myoglobin (CLIA) - Primary ID D-MYO706-AED7

Device Regulatory Overview

The MYO Myoglobin (CLIA) (Model/Catalog Number: MYO706-AE10Y, MYO706-AE10N, MYO706-AE20Y, MYO706-AE20N) is a medical device manufactured by Hangzhou Aichek Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021304 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
MYO706-AE10Y, MYO706-AE10N, MYO706-AE20Y, MYO706-AE20N
Product Code / EMDN
W01021304
Device Name
MYO Myoglobin (CLIA)
Database Sync Date
2026-08-09 16:46:18

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 MYO Myoglobin (CLIA)?

The registered manufacturer of record for MYO Myoglobin (CLIA) is Hangzhou Aichek Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for MYO Myoglobin (CLIA)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-MYO706-AED7.

What classification code is assigned to this device?

This device is registered under product classification code W01021304.

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