GUDIDData
gudid Primary ID: XN-2301SY

Bellema (UDI XN-2301SY)

Manufactured by Guangdong Horigen Mother & Baby Products Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bellema - Primary ID XN-2301SY

Device Regulatory Overview

The Bellema (Model/Catalog Number: XN-2301SY) is a medical device manufactured by Guangdong Horigen Mother & Baby Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HGY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
XN-2301SY
Product Code / EMDN
HGY
Device Name
manual breast pump
Database Sync Date
2026-08-09 09:04:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Bellema?

The registered manufacturer of record for Bellema is Guangdong Horigen Mother & Baby Products Co., Ltd..

What is the Primary UDI-DI identifier for Bellema?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XN-2301SY.

What classification code is assigned to this device?

This device is registered under product classification code HGY.

Similar Classification Devices (HGY)

Other Devices by Guangdong Horigen Mother & Baby Products Co., Ltd.

Programmatic Export

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

JSON API Endpoint