eudamed_udi
Primary ID: 16953611800594
Nuliie (UDI 16953611800594)
Manufactured by Changzhou Dailys Care Products Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nuliie - Primary ID 16953611800594
Device Regulatory Overview
The Nuliie (Model/Catalog Number: RDP130) is a medical device manufactured by Changzhou Dailys Care Products Co.,Ltd. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RDP130
- Product Code / EMDN
- M04010101
- Device Name
- 130mm
- Database Sync Date
- 2026-08-09 16:45:44
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 Nuliie?
The registered manufacturer of record for Nuliie is Changzhou Dailys Care Products Co.,Ltd.
What is the Primary UDI-DI identifier for Nuliie?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16953611800594.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Changzhou Dailys Care Products Co.,Ltd
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