eudamed_udi Primary ID: 03770018808048

Boitier de recharge VitaliTENS (UDI 03770018808048)

Manufactured by SUBLIMED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Boitier de recharge VitaliTENS (Model/Catalog Number: 8703704) is a medical device manufactured by SUBLIMED. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8703704
Product Code / EMDN: Z120601
Device Name: Boitier de recharge VitaliTENS
Database Sync Date: 2026-08-09 18:53:39

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 Boitier de recharge VitaliTENS?

The registered manufacturer of record for Boitier de recharge VitaliTENS is SUBLIMED.

What is the Primary UDI-DI identifier for Boitier de recharge VitaliTENS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770018808048.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Similar Classification Devices (Z120601)

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