GUDIDData
eudamed_udi Primary ID: 06942127849893

Double Pigtail Ureteral Stent (UDI 06942127849893)

Manufactured by Alton (Shanghai) Medical Instruments Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Double Pigtail Ureteral Stent - Primary ID 06942127849893

Device Regulatory Overview

The Double Pigtail Ureteral Stent (Model/Catalog Number: AF-D622T0) is a medical device manufactured by Alton (Shanghai) Medical Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification G03040301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AF-D622T0
Product Code / EMDN
G03040301
Device Name
Double Pigtail Ureteral Stent
Database Sync Date
2026-08-09 16:44:59

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 Double Pigtail Ureteral Stent?

The registered manufacturer of record for Double Pigtail Ureteral Stent is Alton (Shanghai) Medical Instruments Co., Ltd..

What is the Primary UDI-DI identifier for Double Pigtail Ureteral Stent?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942127849893.

What classification code is assigned to this device?

This device is registered under product classification code G03040301.

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