eudamed_udi
Primary ID: 05714880205084
KIT ACTIVE PRO IX EU BG (UDI 05714880205084)
Manufactured by WSAUD A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIT ACTIVE PRO IX EU BG - Primary ID 05714880205084
Device Regulatory Overview
The KIT ACTIVE PRO IX EU BG (Model/Catalog Number: 21027656) is a medical device manufactured by WSAUD A/S. This product is indexed under FDA Product Code / Category Classification Y2145060202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21027656
- Product Code / EMDN
- Y2145060202
- Device Name
- INSTANT FIT
- Database Sync Date
- 2026-08-09 16:44:55
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 KIT ACTIVE PRO IX EU BG?
The registered manufacturer of record for KIT ACTIVE PRO IX EU BG is WSAUD A/S.
What is the Primary UDI-DI identifier for KIT ACTIVE PRO IX EU BG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880205084.
What classification code is assigned to this device?
This device is registered under product classification code Y2145060202.
Similar Classification Devices (Y2145060202)
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