GUDIDData
eudamed_udi Primary ID: 05415174002470

Kim (UDI 05415174002470)

Manufactured by Vermeiren Group

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kim - Primary ID 05415174002470

Device Regulatory Overview

The Kim (Model/Catalog Number: 8002251) is a medical device manufactured by Vermeiren Group. This product is indexed under FDA Product Code / Category Classification Z129003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8002251
Product Code / EMDN
Z129003
Device Name
Kim
Database Sync Date
2026-08-09 17:41:08

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 Kim?

The registered manufacturer of record for Kim is Vermeiren Group.

What is the Primary UDI-DI identifier for Kim?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415174002470.

What classification code is assigned to this device?

This device is registered under product classification code Z129003.

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