eudamed_udi Primary ID: 04719878041492

2FS Sterilization Tyvek Rolls 250mm*100M (UDI 04719878041492)

Manufactured by SterileRight Packaging Mfg.Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 2FS Sterilization Tyvek Rolls 250mm*100M (Model/Catalog Number: P101.01.5806) is a medical device manufactured by SterileRight Packaging Mfg.Inc.. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P101.01.5806
Product Code / EMDN: S01020201
Device Name: Sterilization Tyvek Flat Rolls
Database Sync Date: 2026-08-09 16:29:51

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 2FS Sterilization Tyvek Rolls 250mm*100M?

The registered manufacturer of record for 2FS Sterilization Tyvek Rolls 250mm*100M is SterileRight Packaging Mfg.Inc..

What is the Primary UDI-DI identifier for 2FS Sterilization Tyvek Rolls 250mm*100M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719878041492.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

Similar Classification Devices (S01020201)

Other Devices by SterileRight Packaging Mfg.Inc.

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