GUDIDData
eudamed_udi Primary ID: 04719878041485

2FS Sterilization Tyvek Rolls 200mm*100M (UDI 04719878041485)

Manufactured by SterileRight Packaging Mfg.Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 2FS Sterilization Tyvek Rolls 200mm*100M - Primary ID 04719878041485

Device Regulatory Overview

The 2FS Sterilization Tyvek Rolls 200mm*100M (Model/Catalog Number: P106.01.5805) 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
P106.01.5805
Product Code / EMDN
S01020201
Device Name
Sterilization Tyvek Flat Rolls
Database Sync Date
2026-08-09 16:46:57

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 2FS Sterilization Tyvek Rolls 200mm*100M?

The registered manufacturer of record for 2FS Sterilization Tyvek Rolls 200mm*100M is SterileRight Packaging Mfg.Inc..

What is the Primary UDI-DI identifier for 2FS Sterilization Tyvek Rolls 200mm*100M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719878041485.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

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