gudid
Primary ID: HF18-18/180
ZKSK (UDI HF18-18/180)
Manufactured by Beijing ZKSK Technology Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZKSK - Primary ID HF18-18/180
Device Regulatory Overview
The ZKSK (Model/Catalog Number: HF18-18/180) is a medical device manufactured by Beijing ZKSK Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification KGE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HF18-18/180
- Product Code / EMDN
- KGE
- Device Name
- Disposable Hot Biopsy Forceps
- Database Sync Date
- 2026-08-09 09:24:49
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 ZKSK?
The registered manufacturer of record for ZKSK is Beijing ZKSK Technology Co.,Ltd.
What is the Primary UDI-DI identifier for ZKSK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HF18-18/180.
What classification code is assigned to this device?
This device is registered under product classification code KGE.
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