GUDIDData
gudid Primary ID: ABS

Master (UDI ABS)

Manufactured by Dongguan Maisite Medical Instruments Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Master - Primary ID ABS

Device Regulatory Overview

The Master (Model/Catalog Number: ABS) is a medical device manufactured by Dongguan Maisite Medical Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification BYG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ABS
Product Code / EMDN
BYG
Device Name
Database Sync Date
2026-08-09 09:06:35

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 Master?

The registered manufacturer of record for Master is Dongguan Maisite Medical Instruments Co., Ltd..

What is the Primary UDI-DI identifier for Master?

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

What classification code is assigned to this device?

This device is registered under product classification code BYG.

Similar Classification Devices (BYG)

Other Devices by Dongguan Maisite Medical Instruments Co., Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint