gudid
Primary ID: RS008-11194
PUSEN (UDI RS008-11194)
Manufactured by CORITON Instrument Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PUSEN - Primary ID RS008-11194
Device Regulatory Overview
The PUSEN (Model/Catalog Number: RS008-11194) is a medical device manufactured by CORITON Instrument Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RS008-11194
- Product Code / EMDN
- FOX
- Device Name
- Trolley
- Database Sync Date
- 2026-08-09 09:06:39
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 PUSEN?
The registered manufacturer of record for PUSEN is CORITON Instrument Co.,Ltd.
What is the Primary UDI-DI identifier for PUSEN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RS008-11194.
What classification code is assigned to this device?
This device is registered under product classification code FOX.
Similar Classification Devices (FOX)
Other Devices by CORITON Instrument Co.,Ltd
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