eudamed_udi
Primary ID: 08809327356379
ClearCut Knife (UDI 08809327356379)
Manufactured by FINEMEDIX CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ClearCut Knife - Primary ID 08809327356379
Device Regulatory Overview
The ClearCut Knife (Model/Catalog Number: FM-EK0005-2(1820)B) is a medical device manufactured by FINEMEDIX 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
- FM-EK0005-2(1820)B
- Product Code / EMDN
- K0201010301
- Device Name
- Single-Use Electrosurgical Knife
- Database Sync Date
- 2026-08-09 16:29:06
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ClearCut Knife?
The registered manufacturer of record for ClearCut Knife is FINEMEDIX CO., LTD..
What is the Primary UDI-DI identifier for ClearCut Knife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809327356379.
What classification code is assigned to this device?
This device is registered under product classification code K0201010301.
Similar Classification Devices (K0201010301)
Other Devices by FINEMEDIX CO., LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint