GUDIDData
eudamed_udi Primary ID: 05907080634987

Podwiesie linowe podwójne (UDI 05907080634987)

Manufactured by Si-iS Paweł Wyszyński

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Podwiesie linowe podwójne - Primary ID 05907080634987

Device Regulatory Overview

The Podwiesie linowe podwójne (Model/Catalog Number: 5907080634987) is a medical device manufactured by Si-iS Paweł Wyszyński. This product is indexed under FDA Product Code / Category Classification Y0599 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5907080634987
Product Code / EMDN
Y0599
Device Name
Podwiesie linowe
Database Sync Date
2026-08-09 16:29:07

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 Podwiesie linowe podwójne?

The registered manufacturer of record for Podwiesie linowe podwójne is Si-iS Paweł Wyszyński.

What is the Primary UDI-DI identifier for Podwiesie linowe podwójne?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907080634987.

What classification code is assigned to this device?

This device is registered under product classification code Y0599.

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