gudid Primary ID: 31964

WUSH (UDI 31964)

Manufactured by GUANGDONG OKAY TECHNOLOGY CO.,LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The WUSH (Model/Catalog Number: 31964) is a medical device manufactured by GUANGDONG OKAY TECHNOLOGY CO.,LTD.. This product is indexed under FDA Product Code / Category Classification KYZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 31964
Product Code / EMDN: KYZ
Device Name: Wush Mini DLX GREY,Black wolf-Wush Rechargeable (Deluxe,6 tip,catch cup)-1 x Li-battery 2000mAh,model:18650.With rubberized coating. This device complies with part 18 of FCC rules.
Database Sync Date: 2026-08-09 09:24:44

Full Regulatory Attributes

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{
    "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 WUSH?

The registered manufacturer of record for WUSH is GUANGDONG OKAY TECHNOLOGY CO.,LTD..

What is the Primary UDI-DI identifier for WUSH?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 31964.

What classification code is assigned to this device?

This device is registered under product classification code KYZ.

Similar Classification Devices (KYZ)

Other Devices by GUANGDONG OKAY TECHNOLOGY CO.,LTD.

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