eudamed_udi
Primary ID: 08585003405554
Neoprénová bandáž drieku, PA-1 (UDI 08585003405554)
Manufactured by PROTETIKA, a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neoprénová bandáž drieku, PA-1 - Primary ID 08585003405554
Device Regulatory Overview
The Neoprénová bandáž drieku, PA-1 (Model/Catalog Number: 8585003405554) is a medical device manufactured by PROTETIKA, a.s.. This product is indexed under FDA Product Code / Category Classification Y060308 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8585003405554
- Product Code / EMDN
- Y060308
- Device Name
- Lumbosacral orthose
- Database Sync Date
- 2026-08-09 16:28:46
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 Neoprénová bandáž drieku, PA-1?
The registered manufacturer of record for Neoprénová bandáž drieku, PA-1 is PROTETIKA, a.s..
What is the Primary UDI-DI identifier for Neoprénová bandáž drieku, PA-1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08585003405554.
What classification code is assigned to this device?
This device is registered under product classification code Y060308.
Similar Classification Devices (Y060308)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint