eudamed_udi
Primary ID: 06974566272048
FUSSEN (UDI 06974566272048)
Manufactured by Fussen Technology Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FUSSEN - Primary ID 06974566272048
Device Regulatory Overview
The FUSSEN (Model/Catalog Number: F100 size#2) is a medical device manufactured by Fussen Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z11030402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F100 size#2
- Product Code / EMDN
- Z11030402
- Device Name
- F100 size#2
- Database Sync Date
- 2026-08-09 18:10:17
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 FUSSEN?
The registered manufacturer of record for FUSSEN is Fussen Technology Co., Ltd..
What is the Primary UDI-DI identifier for FUSSEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974566272048.
What classification code is assigned to this device?
This device is registered under product classification code Z11030402.
Similar Classification Devices (Z11030402)
Other Devices by Fussen Technology Co., Ltd.
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