gudid
Primary ID: 5401-10-002
SmartMix Curettes (UDI 5401-10-002)
Manufactured by SUMMIT MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SmartMix Curettes - Primary ID 5401-10-002
Device Regulatory Overview
The SmartMix Curettes (Model/Catalog Number: 5401-10-002) is a medical device manufactured by SUMMIT MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification HTF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5401-10-002
- Product Code / EMDN
- HTF
- Device Name
- Curettes
- Database Sync Date
- 2026-08-09 09:22:51
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 SmartMix Curettes?
The registered manufacturer of record for SmartMix Curettes is SUMMIT MEDICAL LIMITED.
What is the Primary UDI-DI identifier for SmartMix Curettes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5401-10-002.
What classification code is assigned to this device?
This device is registered under product classification code HTF.
Similar Classification Devices (HTF)
Other Devices by SUMMIT MEDICAL LIMITED
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