eudamed_udi
Primary ID: 08585003413016
Pavlíkove remence (UDI 08585003413016)
Manufactured by PROTETIKA, a.s.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pavlíkove remence - Primary ID 08585003413016
Device Regulatory Overview
The Pavlíkove remence (Model/Catalog Number: 8585003413016) is a medical device manufactured by PROTETIKA, a.s.. This product is indexed under FDA Product Code / Category Classification Y061219 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8585003413016
- Product Code / EMDN
- Y061219
- Device Name
- Pavlik harness
- Database Sync Date
- 2026-08-09 16:28:54
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 Pavlíkove remence?
The registered manufacturer of record for Pavlíkove remence is PROTETIKA, a.s..
What is the Primary UDI-DI identifier for Pavlíkove remence?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08585003413016.
What classification code is assigned to this device?
This device is registered under product classification code Y061219.
Similar Classification Devices (Y061219)
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