gudid
Primary ID: F200
FUSSEN (UDI F200)
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 F200
Device Regulatory Overview
The FUSSEN (Model/Catalog Number: F200) is a medical device manufactured by Fussen Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MUH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F200
- Product Code / EMDN
- MUH
- Device Name
- Database Sync Date
- 2026-08-09 09:06:37
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 F200.
What classification code is assigned to this device?
This device is registered under product classification code MUH.
Similar Classification Devices (MUH)
Other Devices by Fussen Technology Co., Ltd.
Programmatic Export
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