GUDIDData
eudamed_udi Primary ID: 06973596010217

Sil-Fixx (UDI 06973596010217)

Manufactured by Conlett Technology Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sil-Fixx - Primary ID 06973596010217

Device Regulatory Overview

The Sil-Fixx (Model/Catalog Number: SF1915) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SF1915
Product Code / EMDN
M04040701
Device Name
Sil-Fixx 1.9cm x 1.5M
Database Sync Date
2026-08-09 17:35:07

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 Sil-Fixx?

The registered manufacturer of record for Sil-Fixx is Conlett Technology Inc.

What is the Primary UDI-DI identifier for Sil-Fixx?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010217.

What classification code is assigned to this device?

This device is registered under product classification code M04040701.

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