GUDIDData
eudamed_udi Primary ID: 04712547611545

PGOTOS Sterilization TYVEK Flat Rolls(IYTR) (UDI 04712547611545)

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 PGOTOS Sterilization TYVEK Flat Rolls(IYTR) - Primary ID 04712547611545

Device Regulatory Overview

The PGOTOS Sterilization TYVEK Flat Rolls(IYTR) (Model/Catalog Number: IYTR-300mmX100M) is a medical device manufactured by I YUEH MEDICAL TECHNOLOGY CO., LTD.. This product is indexed under FDA Product Code / Category Classification S01020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
IYTR-300mmX100M
Product Code / EMDN
S01020201
Device Name
Medical Sterilization Package
Database Sync Date
2026-08-09 16:29:00

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of PGOTOS Sterilization TYVEK Flat Rolls(IYTR)?

The registered manufacturer of record for PGOTOS Sterilization TYVEK Flat Rolls(IYTR) is I YUEH MEDICAL TECHNOLOGY CO., LTD..

What is the Primary UDI-DI identifier for PGOTOS Sterilization TYVEK Flat Rolls(IYTR)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04712547611545.

What classification code is assigned to this device?

This device is registered under product classification code S01020201.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint