SEJOY (UDI DBP-2208)

Manufactured by JOYTECH HEALTHCARE CO.,LTD

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SEJOY (Model/Catalog Number: DBP-2208) is a medical device manufactured by JOYTECH HEALTHCARE CO.,LTD. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DBP-2208
Product Code / EMDN: DXN
Device Name
Database Sync Date: 2026-08-09 09:06:49

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 SEJOY?

The registered manufacturer of record for SEJOY is JOYTECH HEALTHCARE CO.,LTD.

What is the Primary UDI-DI identifier for SEJOY?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DBP-2208.

What classification code is assigned to this device?

This device is registered under product classification code DXN.

Similar Classification Devices (DXN)

Other Devices by JOYTECH HEALTHCARE CO.,LTD

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