GUDIDData
gudid Primary ID: AOSS-50B

Amazewell (UDI AOSS-50B)

Manufactured by Guangzhou Decheng Biotechnology Co., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amazewell - Primary ID AOSS-50B

Device Regulatory Overview

The Amazewell (Model/Catalog Number: AOSS-50B) is a medical device manufactured by Guangzhou Decheng Biotechnology Co., LTD. This product is indexed under FDA Product Code / Category Classification NGE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AOSS-50B
Product Code / EMDN
NGE
Device Name
Amazewell Ovulation Rapid Test Strip, 50T/Box
Database Sync Date
2026-08-09 09:37:39

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 Amazewell?

The registered manufacturer of record for Amazewell is Guangzhou Decheng Biotechnology Co., LTD.

What is the Primary UDI-DI identifier for Amazewell?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AOSS-50B.

What classification code is assigned to this device?

This device is registered under product classification code NGE.

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