eudamed_udi
Primary ID: 08809483601009
Neofect Smart Kids (UDI 08809483601009)
Manufactured by Dynamic solution Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neofect Smart Kids - Primary ID 08809483601009
Device Regulatory Overview
The Neofect Smart Kids (Model/Catalog Number: KDCA4L) is a medical device manufactured by Dynamic solution Co., Ltd. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KDCA4L
- Product Code / EMDN
- Z12069099
- Device Name
- Neofect Smart Kids
- Database Sync Date
- 2026-08-09 16:29:48
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 Neofect Smart Kids?
The registered manufacturer of record for Neofect Smart Kids is Dynamic solution Co., Ltd.
What is the Primary UDI-DI identifier for Neofect Smart Kids?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809483601009.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by Dynamic solution Co., Ltd
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