GUDIDData
eudamed_udi Primary ID: 04712547611620

PROTOS Sterilization TYVEK Pouches(IYTP) (UDI 04712547611620)

Manufactured by I YUEH MEDICAL TECHNOLOGY CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROTOS Sterilization TYVEK Pouches(IYTP) - Primary ID 04712547611620

Device Regulatory Overview

The PROTOS Sterilization TYVEK Pouches(IYTP) (Model/Catalog Number: IYTP-200X300mm) is a medical device manufactured by I YUEH MEDICAL TECHNOLOGY CO., LTD.. This product is indexed under FDA Product Code / Category Classification S01010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IYTP-200X300mm
Product Code / EMDN
S01010201
Device Name
Medical Sterilization Package
Database Sync Date
2026-08-09 16:50:56

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 PROTOS Sterilization TYVEK Pouches(IYTP)?

The registered manufacturer of record for PROTOS Sterilization TYVEK Pouches(IYTP) is I YUEH MEDICAL TECHNOLOGY CO., LTD..

What is the Primary UDI-DI identifier for PROTOS Sterilization TYVEK Pouches(IYTP)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712547611620.

What classification code is assigned to this device?

This device is registered under product classification code S01010201.

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