gudid
Primary ID: US31B-12
EUScope (UDI US31B-12)
Manufactured by Shanghai AnQing Medical Instrument Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EUScope - Primary ID US31B-12
Device Regulatory Overview
The EUScope (Model/Catalog Number: US31B-12) is a medical device manufactured by Shanghai AnQing Medical Instrument Co., Ltd. This product is indexed under FDA Product Code / Category Classification FGB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- US31B-12
- Product Code / EMDN
- FGB
- Device Name
- Flexible Ureterorenoscope is a flexible inserted portion intended for visual examination and treatment of the ureter.Only be used with the designed DOSTM video processor approved by SHANGHAI ANQING.
- Database Sync Date
- 2026-08-09 09:05:22
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 EUScope?
The registered manufacturer of record for EUScope is Shanghai AnQing Medical Instrument Co., Ltd.
What is the Primary UDI-DI identifier for EUScope?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is US31B-12.
What classification code is assigned to this device?
This device is registered under product classification code FGB.
Similar Classification Devices (FGB)
Other Devices by Shanghai AnQing Medical Instrument Co., Ltd
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