eudamed_udi Primary ID: 06438263910271

STERIKING® Super Crepe Blue (UDI 06438263910271)

Manufactured by Wipak Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The STERIKING® Super Crepe Blue (Model/Catalog Number: SCB100/140) is a medical device manufactured by Wipak Oy. This product is indexed under FDA Product Code / Category Classification S010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SCB100/140
Product Code / EMDN: S010301
Device Name: STERIKING® Wraps
Database Sync Date: 2026-08-09 16:28:53

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® Super Crepe Blue?

The registered manufacturer of record for STERIKING® Super Crepe Blue is Wipak Oy.

What is the Primary UDI-DI identifier for STERIKING® Super Crepe Blue?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438263910271.

What classification code is assigned to this device?

This device is registered under product classification code S010301.

Similar Classification Devices (S010301)

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