GUDIDData
eudamed_udi Primary ID: 06973596010385

Sonic Muffs (UDI 06973596010385)

Manufactured by Conlett Technology Inc

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sonic Muffs - Primary ID 06973596010385

Device Regulatory Overview

The Sonic Muffs (Model/Catalog Number: SM-001) is a medical device manufactured by Conlett Technology Inc. This product is indexed under FDA Product Code / Category Classification T0399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SM-001
Product Code / EMDN
T0399
Device Name
Sonic Muffs
Database Sync Date
2026-08-09 18:40:30

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 Sonic Muffs?

The registered manufacturer of record for Sonic Muffs is Conlett Technology Inc.

What is the Primary UDI-DI identifier for Sonic Muffs?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973596010385.

What classification code is assigned to this device?

This device is registered under product classification code T0399.

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