Single-use Ureteral Access Sheath (UDI Y-10-45)
Manufactured by Shenzhen HugeMed Medical Technical Development Co., Ltd.
Device Regulatory Overview
The Single-use Ureteral Access Sheath (Model/Catalog Number: Y-10-45) is a medical device manufactured by Shenzhen HugeMed Medical Technical Development Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Y-10-45
- Product Code / EMDN
- FED
- Device Name
- Database Sync Date
- 2026-08-09 09:06:47
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 Single-use Ureteral Access Sheath?
The registered manufacturer of record for Single-use Ureteral Access Sheath is Shenzhen HugeMed Medical Technical Development Co., Ltd..
What is the Primary UDI-DI identifier for Single-use Ureteral Access Sheath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Y-10-45.
What classification code is assigned to this device?
This device is registered under product classification code FED.
Similar Classification Devices (FED)
Other Devices by Shenzhen HugeMed Medical Technical Development Co., Ltd.
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