eudamed_udi
Primary ID: 04038155622354
Polster Skoliosebügel schräg (UDI 04038155622354)
Manufactured by TIGGES-Zours GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Polster Skoliosebügel schräg - Primary ID 04038155622354
Device Regulatory Overview
The Polster Skoliosebügel schräg (Model/Catalog Number: 62235schw/gra) 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
- 62235schw/gra
- Product Code / EMDN
- Y060380
- Device Name
- TIGGES/T-FLEX
- Database Sync Date
- 2026-08-09 16:30:28
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 Polster Skoliosebügel schräg?
The registered manufacturer of record for Polster Skoliosebügel schräg is TIGGES-Zours GmbH.
What is the Primary UDI-DI identifier for Polster Skoliosebügel schräg?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04038155622354.
What classification code is assigned to this device?
This device is registered under product classification code Y060380.
Similar Classification Devices (Y060380)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint