gudid
Primary ID: G9901
Premium Plus (UDI G9901)
Manufactured by Premium Plus (Dongguan) Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Premium Plus - Primary ID G9901
Device Regulatory Overview
The Premium Plus (Model/Catalog Number: G9901) is a medical device manufactured by Premium Plus (Dongguan) Limited. This product is indexed under FDA Product Code / Category Classification KXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G9901
- Product Code / EMDN
- KXR
- Device Name
- Micro Applicators
- Database Sync Date
- 2026-08-09 09:01:55
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 Premium Plus?
The registered manufacturer of record for Premium Plus is Premium Plus (Dongguan) Limited.
What is the Primary UDI-DI identifier for Premium Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G9901.
What classification code is assigned to this device?
This device is registered under product classification code KXR.
Similar Classification Devices (KXR)
Other Devices by Premium Plus (Dongguan) Limited
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