eudamed_udi
Primary ID: 08585003403741
Bandáž stehna, neoprén, ST-1/25 L, ľavá (UDI 08585003403741)
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 L, ľavá - Primary ID 08585003403741
Device Regulatory Overview
The Bandáž stehna, neoprén, ST-1/25 L, ľavá (Model/Catalog Number: 8585003403741) 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
- 8585003403741
- Product Code / EMDN
- Y061217
- Device Name
- Thigh orthose
- Database Sync Date
- 2026-08-09 17:18:55
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Bandáž stehna, neoprén, ST-1/25 L, ľavá?
The registered manufacturer of record for Bandáž stehna, neoprén, ST-1/25 L, ľavá is PROTETIKA, a.s..
What is the Primary UDI-DI identifier for Bandáž stehna, neoprén, ST-1/25 L, ľavá?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08585003403741.
What classification code is assigned to this device?
This device is registered under product classification code Y061217.
Similar Classification Devices (Y061217)
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