eudamed_udi
Primary ID: 06973661910060
SKL (UDI 06973661910060)
Manufactured by Guangdong SKL Medical Instrument Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SKL - Primary ID 06973661910060
Device Regulatory Overview
The SKL (Model/Catalog Number: L3) is a medical device manufactured by Guangdong SKL Medical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification L159009 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L3
- Product Code / EMDN
- L159009
- Device Name
- Ultrasonic scaler
- Database Sync Date
- 2026-08-09 16:30:40
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 SKL?
The registered manufacturer of record for SKL is Guangdong SKL Medical Instrument Co.,Ltd..
What is the Primary UDI-DI identifier for SKL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973661910060.
What classification code is assigned to this device?
This device is registered under product classification code L159009.
Similar Classification Devices (L159009)
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