gudid Primary ID: AS8012

No (UDI AS8012)

Manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The No (Model/Catalog Number: AS8012) is a medical device manufactured by Shenzhen Jian Feng Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NGX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AS8012
Product Code / EMDN: NGX
Device Name
Database Sync Date: 2026-08-09 09:06:39

Full Regulatory Attributes

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{
    "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 No?

The registered manufacturer of record for No is Shenzhen Jian Feng Electronic Technology Co., Ltd..

What is the Primary UDI-DI identifier for No?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AS8012.

What classification code is assigned to this device?

This device is registered under product classification code NGX.

Similar Classification Devices (NGX)

Other Devices by Shenzhen Jian Feng Electronic Technology Co., Ltd.

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