GUDIDData
gudid Primary ID: 10CFS07030

Avenir (UDI 10CFS07030)

Manufactured by Shanghai Wallaby Medical Technologies Co., Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Avenir - Primary ID 10CFS07030

Device Regulatory Overview

The Avenir (Model/Catalog Number: 10CFS07030) is a medical device manufactured by Shanghai Wallaby Medical Technologies Co., Inc.. This product is indexed under FDA Product Code / Category Classification KRD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10CFS07030
Product Code / EMDN
KRD
Device Name
Embolic Coil
Database Sync Date
2026-08-09 09:06:45

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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Frequently Asked Questions

Who is the primary manufacturer of Avenir?

The registered manufacturer of record for Avenir is Shanghai Wallaby Medical Technologies Co., Inc..

What is the Primary UDI-DI identifier for Avenir?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10CFS07030.

What classification code is assigned to this device?

This device is registered under product classification code KRD.

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