eudamed_udi
Primary ID: 00841494105198
LLETZ Loop Electrode (UDI 00841494105198)
Manufactured by Cynosure LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LLETZ Loop Electrode - Primary ID 00841494105198
Device Regulatory Overview
The LLETZ Loop Electrode (Model/Catalog Number: W3D) is a medical device manufactured by Cynosure LLC. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W3D
- Product Code / EMDN
- K0201010301
- Device Name
- LLETZ Loop Electrode
- Database Sync Date
- 2026-08-09 16:29:00
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 LLETZ Loop Electrode?
The registered manufacturer of record for LLETZ Loop Electrode is Cynosure LLC.
What is the Primary UDI-DI identifier for LLETZ Loop Electrode?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00841494105198.
What classification code is assigned to this device?
This device is registered under product classification code K0201010301.
Similar Classification Devices (K0201010301)
Other Devices by Cynosure LLC
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