Alleset (UDI 25-0200)
Manufactured by GRI Medical & Electronic Technology Co., Ltd.
Device Regulatory Overview
The Alleset (Model/Catalog Number: 25-0200) is a medical device manufactured by GRI Medical & Electronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification KXF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 25-0200
- Product Code / EMDN
- KXF
- Device Name
- Pad_Cautery Pencil_No-sterilize_2000ea/cs
- Database Sync Date
- 2026-08-09 09:22:03
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 Alleset?
The registered manufacturer of record for Alleset is GRI Medical & Electronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Alleset?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 25-0200.
What classification code is assigned to this device?
This device is registered under product classification code KXF.
Similar Classification Devices (KXF)
Other Devices by GRI Medical & Electronic Technology Co., Ltd.
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