eudamed_udi
Primary ID: 08809306764669
Octopus RF electrode (UDI 08809306764669)
Manufactured by STARmed Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Octopus RF electrode - Primary ID 08809306764669
Device Regulatory Overview
The Octopus RF electrode (Model/Catalog Number: 15-15P2535_V2-Duo) is a medical device manufactured by STARmed Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 15-15P2535_V2-Duo
- Product Code / EMDN
- K0201010301
- Device Name
- Octopus RF electrode
- Database Sync Date
- 2026-08-09 16:29:09
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 Octopus RF electrode?
The registered manufacturer of record for Octopus RF electrode is STARmed Co., Ltd..
What is the Primary UDI-DI identifier for Octopus RF electrode?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809306764669.
What classification code is assigned to this device?
This device is registered under product classification code K0201010301.
Similar Classification Devices (K0201010301)
Other Devices by STARmed Co., Ltd.
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