GUDIDData
eudamed_udi Primary ID: 06974610341515

STERIKING® See-Through Heat-Sealable Pouches (UDI 06974610341515)

Manufactured by Wipak Packaging (Changshu) Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERIKING® See-Through Heat-Sealable Pouches - Primary ID 06974610341515

Device Regulatory Overview

The STERIKING® See-Through Heat-Sealable Pouches (Model/Catalog Number: S14; S14-3P) is a medical device manufactured by Wipak Packaging (Changshu) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S14; S14-3P
Product Code / EMDN
S01010101
Device Name
STERIKING® Pouches and Rolls
Database Sync Date
2026-08-09 16:29:55

Full Regulatory Attributes

🔒 Token Gated
{
    "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® See-Through Heat-Sealable Pouches?

The registered manufacturer of record for STERIKING® See-Through Heat-Sealable Pouches is Wipak Packaging (Changshu) Co., Ltd..

What is the Primary UDI-DI identifier for STERIKING® See-Through Heat-Sealable Pouches?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974610341515.

What classification code is assigned to this device?

This device is registered under product classification code S01010101.

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