gudid Primary ID: ZHF-IPL-III

GOODWIND (UDI ZHF-IPL-III)

Manufactured by Shenzhen Goodwind technology development Co.,Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The GOODWIND (Model/Catalog Number: ZHF-IPL-III) is a medical device manufactured by Shenzhen Goodwind technology development Co.,Ltd. This product is indexed under FDA Product Code / Category Classification OHT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ZHF-IPL-III
Product Code / EMDN: OHT
Device Name: IPL Hair Removal Device
Database Sync Date: 2026-08-09 09:05:24

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 GOODWIND?

The registered manufacturer of record for GOODWIND is Shenzhen Goodwind technology development Co.,Ltd.

What is the Primary UDI-DI identifier for GOODWIND?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ZHF-IPL-III.

What classification code is assigned to this device?

This device is registered under product classification code OHT.

Similar Classification Devices (OHT)

Other Devices by Shenzhen Goodwind technology development Co.,Ltd

Programmatic Export

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

JSON API Endpoint