Steriking (UDI SS-T1)

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: SS-T1) is a medical device manufactured by Wipak Oy. This product is indexed under FDA Product Code / Category Classification FRG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SS-T1
Product Code / EMDN: FRG
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 SS-T1.

What classification code is assigned to this device?

This device is registered under product classification code FRG.

Similar Classification Devices (FRG)

Other Devices by Wipak Oy

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