gudid Primary ID: X-007.99.396

BETA 4 NT RECHARGEABLE HANDLE (UDI X-007.99.396)

Manufactured by SONTEC INSTRUMENTS, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BETA 4 NT RECHARGEABLE HANDLE (Model/Catalog Number: X-007.99.396) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HLJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: X-007.99.396
Product Code / EMDN: HLJ
Device Name: BETA 4 NT RECHARGEABLE HANDLE
Database Sync Date: 2026-08-09 09:07:02

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 BETA 4 NT RECHARGEABLE HANDLE?

The registered manufacturer of record for BETA 4 NT RECHARGEABLE HANDLE is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for BETA 4 NT RECHARGEABLE HANDLE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is X-007.99.396.

What classification code is assigned to this device?

This device is registered under product classification code HLJ.

Similar Classification Devices (HLJ)

Other Devices by SONTEC INSTRUMENTS, INC.

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