eudamed_udi
Primary ID: 08585063861734
Ortéza zápěstí ZA-741, pravá (UDI 08585063861734)
Manufactured by PROTETIKA, a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ortéza zápěstí ZA-741, pravá - Primary ID 08585063861734
Device Regulatory Overview
The Ortéza zápěstí ZA-741, pravá (Model/Catalog Number: 8585063861734) is a medical device manufactured by PROTETIKA, a.s.. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8585063861734
- Product Code / EMDN
- Y060612
- Device Name
- Wrist orthose
- Database Sync Date
- 2026-08-09 16:46:13
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 Ortéza zápěstí ZA-741, pravá?
The registered manufacturer of record for Ortéza zápěstí ZA-741, pravá is PROTETIKA, a.s..
What is the Primary UDI-DI identifier for Ortéza zápěstí ZA-741, pravá?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08585063861734.
What classification code is assigned to this device?
This device is registered under product classification code Y060612.
Similar Classification Devices (Y060612)
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