eudamed_udi
Primary ID: 06943532400556
TERMOK (UDI 06943532400556)
Manufactured by Kangfu Medical Equipment Factory
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TERMOK - Primary ID 06943532400556
Device Regulatory Overview
The TERMOK (Model/Catalog Number: KFT-22M/6943532400556) is a medical device manufactured by Kangfu Medical Equipment Factory. This product is indexed under FDA Product Code / Category Classification V0301010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KFT-22M/6943532400556
- Product Code / EMDN
- V0301010202
- Device Name
- Infrared thermometer
- Database Sync Date
- 2026-08-09 18:12:20
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 TERMOK?
The registered manufacturer of record for TERMOK is Kangfu Medical Equipment Factory.
What is the Primary UDI-DI identifier for TERMOK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06943532400556.
What classification code is assigned to this device?
This device is registered under product classification code V0301010202.
Similar Classification Devices (V0301010202)
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