GUDIDData
gudid Primary ID: KINDviano 5 RIC 312

KIND (UDI KINDviano 5 RIC 312)

Manufactured by Starkey Laboratories, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIND - Primary ID KINDviano 5 RIC 312

Device Regulatory Overview

The KIND (Model/Catalog Number: KINDviano 5 RIC 312) is a medical device manufactured by Starkey Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification KLW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KINDviano 5 RIC 312
Product Code / EMDN
KLW
Device Name
Database Sync Date
2026-08-09 09:07:49

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 KIND?

The registered manufacturer of record for KIND is Starkey Laboratories, Inc..

What is the Primary UDI-DI identifier for KIND?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KINDviano 5 RIC 312.

What classification code is assigned to this device?

This device is registered under product classification code KLW.

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