gudid
Primary ID: 1.010.2333
SURGmatic S201 XC (UDI 1.010.2333)
Manufactured by KaVo Dental GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SURGmatic S201 XC - Primary ID 1.010.2333
Device Regulatory Overview
The SURGmatic S201 XC (Model/Catalog Number: 1.010.2333) is a medical device manufactured by KaVo Dental GmbH. This product is indexed under FDA Product Code / Category Classification EBW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1.010.2333
- Product Code / EMDN
- EBW
- Device Name
- This is a medical device.This is a medical device.
- Database Sync Date
- 2026-08-09 09:08:27
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 SURGmatic S201 XC?
The registered manufacturer of record for SURGmatic S201 XC is KaVo Dental GmbH.
What is the Primary UDI-DI identifier for SURGmatic S201 XC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.010.2333.
What classification code is assigned to this device?
This device is registered under product classification code EBW.
Similar Classification Devices (EBW)
Other Devices by KaVo Dental GmbH
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