eudamed_udi Primary ID: 06438263910028

STERIKING® Crepe Papers (UDI 06438263910028)

Manufactured by Wipak Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The STERIKING® Crepe Papers (Model/Catalog Number: SPC50W) 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: SPC50W
Product Code / EMDN: S010301
Device Name: STERIKING® Wraps
Database Sync Date: 2026-08-09 16:46:29

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® Crepe Papers?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438263910028.

What classification code is assigned to this device?

This device is registered under product classification code S010301.

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