eudamed_udi
Primary ID: 08585003403703
Bandáž stehna, neoprén, ST-1/25 P, pravá (UDI 08585003403703)
Manufactured by PROTETIKA, a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bandáž stehna, neoprén, ST-1/25 P, pravá - Primary ID 08585003403703
Device Regulatory Overview
The Bandáž stehna, neoprén, ST-1/25 P, pravá (Model/Catalog Number: 8585003403703) is a medical device manufactured by PROTETIKA, a.s.. This product is indexed under FDA Product Code / Category Classification Y061217 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8585003403703
- Product Code / EMDN
- Y061217
- Device Name
- Thigh orthose
- Database Sync Date
- 2026-08-09 16:29:14
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 Bandáž stehna, neoprén, ST-1/25 P, pravá?
The registered manufacturer of record for Bandáž stehna, neoprén, ST-1/25 P, pravá is PROTETIKA, a.s..
What is the Primary UDI-DI identifier for Bandáž stehna, neoprén, ST-1/25 P, pravá?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08585003403703.
What classification code is assigned to this device?
This device is registered under product classification code Y061217.
Similar Classification Devices (Y061217)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint