eudamed_udi
Primary ID: 05714880237610
KIT ACTIVE IX EU BLK (UDI 05714880237610)
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 IX EU BLK - Primary ID 05714880237610
Device Regulatory Overview
The KIT ACTIVE IX EU BLK (Model/Catalog Number: 21021960) 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
- 21021960
- Product Code / EMDN
- Y2145060202
- Device Name
- INSTANT FIT
- Database Sync Date
- 2026-08-09 16:45:04
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 IX EU BLK?
The registered manufacturer of record for KIT ACTIVE IX EU BLK is WSAUD A/S.
What is the Primary UDI-DI identifier for KIT ACTIVE IX EU BLK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05714880237610.
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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