Unspecified Brand (UDI 06974269824902)
Manufactured by Baihe Medical Technology (Wuhan) Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: REF) is a medical device manufactured by Baihe Medical Technology (Wuhan) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification U020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- REF
- Product Code / EMDN
- U020302
- Device Name
- Ureteral Stents
- Database Sync Date
- 2026-08-09 16:28:55
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Baihe Medical Technology (Wuhan) Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974269824902.
What classification code is assigned to this device?
This device is registered under product classification code U020302.
Similar Classification Devices (U020302)
Other Devices by Baihe Medical Technology (Wuhan) Co., Ltd.
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