GUDIDData
gudid Primary ID: VC-075-010-PL

VISICOIL (UDI VC-075-010-PL)

Manufactured by Izi Medical Products, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISICOIL - Primary ID VC-075-010-PL

Device Regulatory Overview

The VISICOIL (Model/Catalog Number: VC-075-010-PL) is a medical device manufactured by Izi Medical Products, LLC. This product is indexed under FDA Product Code / Category Classification IYE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VC-075-010-PL
Product Code / EMDN
IYE
Device Name
0.75mm x 1.0cm VISICOIL loaded in an 18 gauge pre-waxed brachytherapy needle.
Database Sync Date
2026-08-09 09:06:21

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 VISICOIL?

The registered manufacturer of record for VISICOIL is Izi Medical Products, LLC.

What is the Primary UDI-DI identifier for VISICOIL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VC-075-010-PL.

What classification code is assigned to this device?

This device is registered under product classification code IYE.

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