GUDIDData
eudamed_udi Primary ID: 04038155627250

Schultergurte (UDI 04038155627250)

Manufactured by TIGGES-Zours GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Schultergurte - Primary ID 04038155627250

Device Regulatory Overview

The Schultergurte (Model/Catalog Number: 62725schwarz) is a medical device manufactured by TIGGES-Zours GmbH. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
62725schwarz
Product Code / EMDN
Y060380
Device Name
TIGGES/T-FLEX
Database Sync Date
2026-08-09 16:47:03

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 Schultergurte?

The registered manufacturer of record for Schultergurte is TIGGES-Zours GmbH.

What is the Primary UDI-DI identifier for Schultergurte?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04038155627250.

What classification code is assigned to this device?

This device is registered under product classification code Y060380.

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