GUDIDData
eudamed_udi Primary ID: 06973536540583

119102I041147 (UDI 06973536540583)

Manufactured by Foshan HCT Medical Equipment Co.,ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 119102I041147 - Primary ID 06973536540583

Device Regulatory Overview

The 119102I041147 (Model/Catalog Number: 24712/HCT-9102B RED) is a medical device manufactured by Foshan HCT Medical Equipment Co.,ltd. This product is indexed under FDA Product Code / Category Classification Y120612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
24712/HCT-9102B RED
Product Code / EMDN
Y120612
Device Name
rollator
Database Sync Date
2026-08-09 16:29:56

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 119102I041147?

The registered manufacturer of record for 119102I041147 is Foshan HCT Medical Equipment Co.,ltd.

What is the Primary UDI-DI identifier for 119102I041147?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973536540583.

What classification code is assigned to this device?

This device is registered under product classification code Y120612.

Programmatic Export

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

JSON API Endpoint