eudamed_udi
Primary ID: 05903684800087
WKS (UDI 05903684800087)
Manufactured by MEDEN-INMED SP. Z O.O.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for WKS - Primary ID 05903684800087
Device Regulatory Overview
The WKS (Model/Catalog Number: -) is a medical device manufactured by MEDEN-INMED SP. Z O.O.. This product is indexed under FDA Product Code / Category Classification Z120618 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- -
- Product Code / EMDN
- Z120618
- Device Name
- Urządzenie do masażu wirowego
- Database Sync Date
- 2026-08-09 16:46:41
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 WKS?
The registered manufacturer of record for WKS is MEDEN-INMED SP. Z O.O..
What is the Primary UDI-DI identifier for WKS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05903684800087.
What classification code is assigned to this device?
This device is registered under product classification code Z120618.
Similar Classification Devices (Z120618)
Other Devices by MEDEN-INMED SP. Z O.O.
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