eudamed_udi Primary ID: D-3159921201311WU

NUK (UDI D-3159921201311WU)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NUK (Model/Catalog Number: 80891099) is a medical device manufactured by Radiant Innovation Inc.. This product is indexed under FDA Product Code / Category Classification V0301010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 80891099
Product Code / EMDN: V0301010202
Device Name: THI0KZ
Database Sync Date: 2026-08-09 16:50:54

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 NUK?

The registered manufacturer of record for NUK is Radiant Innovation Inc..

What is the Primary UDI-DI identifier for NUK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-3159921201311WU.

What classification code is assigned to this device?

This device is registered under product classification code V0301010202.

Similar Classification Devices (V0301010202)

Other Devices by Radiant Innovation Inc.

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