Steriking (UDI R42)

Manufactured by Wipak Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Steriking (Model/Catalog Number: R42) is a medical device manufactured by Wipak Oy. This product is indexed under FDA Product Code / Category Classification KCT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: R42
Product Code / EMDN: KCT
Device Name: Single use sterilization packaging
Database Sync Date: 2026-08-09 09:24:54

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 Steriking?

The registered manufacturer of record for Steriking is Wipak Oy.

What is the Primary UDI-DI identifier for Steriking?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R42.

What classification code is assigned to this device?

This device is registered under product classification code KCT.

Similar Classification Devices (KCT)

Other Devices by Wipak Oy

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