eudamed_udi
Primary ID: 05907813382949
Kostka rehab. 40x40x40 - K012 (UDI 05907813382949)
Manufactured by HABYS Sp. z o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kostka rehab. 40x40x40 - K012 - Primary ID 05907813382949
Device Regulatory Overview
The Kostka rehab. 40x40x40 - K012 (Model/Catalog Number: G-KSKOK012001) is a medical device manufactured by HABYS Sp. z o.o.. This product is indexed under FDA Product Code / Category Classification Z120602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G-KSKOK012001
- Product Code / EMDN
- Z120602
- Device Name
- kształtki rehabilitacyjne
- Database Sync Date
- 2026-08-09 16:28:46
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 Kostka rehab. 40x40x40 - K012?
The registered manufacturer of record for Kostka rehab. 40x40x40 - K012 is HABYS Sp. z o.o..
What is the Primary UDI-DI identifier for Kostka rehab. 40x40x40 - K012?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907813382949.
What classification code is assigned to this device?
This device is registered under product classification code Z120602.
Similar Classification Devices (Z120602)
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