GUDIDData
gudid Primary ID: UA-S1802

Single-use Ureteral Access Sheath (UDI UA-S1802)

Manufactured by Hunan Vathin Medical Instrument Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Single-use Ureteral Access Sheath - Primary ID UA-S1802

Device Regulatory Overview

The Single-use Ureteral Access Sheath (Model/Catalog Number: UA-S1802) is a medical device manufactured by Hunan Vathin Medical Instrument 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
UA-S1802
Product Code / EMDN
FED
Device Name
Database Sync Date
2026-08-09 09:06:41

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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 Hunan Vathin Medical Instrument 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 UA-S1802.

What classification code is assigned to this device?

This device is registered under product classification code FED.

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