eudamed_udi
Primary ID: 06973740150172
Kinetik (UDI 06973740150172)
Manufactured by Huai An Hua Lve Electronics Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kinetik - Primary ID 06973740150172
Device Regulatory Overview
The Kinetik (Model/Catalog Number: IET4PC) is a medical device manufactured by Huai An Hua Lve Electronics Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification T030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IET4PC
- Product Code / EMDN
- T030199
- Device Name
- Disposable probe covers
- Database Sync Date
- 2026-08-09 18:44:53
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 Kinetik?
The registered manufacturer of record for Kinetik is Huai An Hua Lve Electronics Co.,Ltd..
What is the Primary UDI-DI identifier for Kinetik?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973740150172.
What classification code is assigned to this device?
This device is registered under product classification code T030199.
Similar Classification Devices (T030199)
Other Devices by Huai An Hua Lve Electronics Co.,Ltd.
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