GUDIDData
gudid Primary ID: 21055

Bynex (UDI 21055)

Manufactured by Shaoxing Haoshide Medical Products Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bynex - Primary ID 21055

Device Regulatory Overview

The Bynex (Model/Catalog Number: 21055) is a medical device manufactured by Shaoxing Haoshide Medical Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification PQE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
21055
Product Code / EMDN
PQE
Device Name
Two-piece ostomy bag Flat Wafer 10 pieces/box 15 boxes/carton
Database Sync Date
2026-08-09 09:05:26

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 Bynex?

The registered manufacturer of record for Bynex is Shaoxing Haoshide Medical Products Co., Ltd..

What is the Primary UDI-DI identifier for Bynex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21055.

What classification code is assigned to this device?

This device is registered under product classification code PQE.

Similar Classification Devices (PQE)

Other Devices by Shaoxing Haoshide Medical Products Co., Ltd.

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