eudamed_udi
Primary ID: 06970384255317
Tourniquet (UDI 06970384255317)
Manufactured by HONSUN (NANTONG) Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tourniquet - Primary ID 06970384255317
Device Regulatory Overview
The Tourniquet (Model/Catalog Number: HS-403C) is a medical device manufactured by HONSUN (NANTONG) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V9003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HS-403C
- Product Code / EMDN
- V9003
- Device Name
- Tourniquet
- Database Sync Date
- 2026-08-09 16:30:38
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 Tourniquet?
The registered manufacturer of record for Tourniquet is HONSUN (NANTONG) Co., Ltd..
What is the Primary UDI-DI identifier for Tourniquet?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970384255317.
What classification code is assigned to this device?
This device is registered under product classification code V9003.
Similar Classification Devices (V9003)
Other Devices by HONSUN (NANTONG) Co., Ltd.
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