GUDIDData
eudamed_udi Primary ID: 08806182202476

Serach Port (UDI 08806182202476)

Manufactured by SEJONG MEDICAL Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Serach Port - Primary ID 08806182202476

Device Regulatory Overview

The Serach Port (Model/Catalog Number: WR-21-6060) is a medical device manufactured by SEJONG MEDICAL Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01020106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
WR-21-6060
Product Code / EMDN
K01020106
Device Name
Serach Port
Database Sync Date
2026-08-09 17:18:01

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 Serach Port?

The registered manufacturer of record for Serach Port is SEJONG MEDICAL Co., Ltd..

What is the Primary UDI-DI identifier for Serach Port?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806182202476.

What classification code is assigned to this device?

This device is registered under product classification code K01020106.

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