Reamer (UDI 06936340010390)
Manufactured by Shandong Hengfeng Kerui Medical Equipment Co., Ltd
Device Regulatory Overview
The Reamer (Model/Catalog Number: SSR 2102 130) is a medical device manufactured by Shandong Hengfeng Kerui Medical Equipment Co., Ltd. This product is indexed under FDA Product Code / Category Classification Q01010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SSR 2102 130
- Product Code / EMDN
- Q01010299
- Device Name
- Dental Root Canal Instruments
- Database Sync Date
- 2026-08-09 16:29:35
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 Reamer?
The registered manufacturer of record for Reamer is Shandong Hengfeng Kerui Medical Equipment Co., Ltd.
What is the Primary UDI-DI identifier for Reamer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936340010390.
What classification code is assigned to this device?
This device is registered under product classification code Q01010299.
Similar Classification Devices (Q01010299)
Other Devices by Shandong Hengfeng Kerui Medical Equipment Co., Ltd
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