eudamed_udi Primary ID: 03770018808062

VitaliTENS (UDI 03770018808062)

Manufactured by sublimed

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

Scannable UDI-DI Representation

Device Regulatory Overview

The VitaliTENS (Model/Catalog Number: 8703648) 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: 8703648
Product Code / EMDN: Z120601
Device Name: actiTENS kit / actiTENS mini kit / coffret VitaliTENS/ coffret VitaliTENS mini
Database Sync Date: 2026-08-09 16:58:58

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 VitaliTENS?

The registered manufacturer of record for VitaliTENS is sublimed.

What is the Primary UDI-DI identifier for VitaliTENS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770018808062.

What classification code is assigned to this device?

This device is registered under product classification code Z120601.

Similar Classification Devices (Z120601)

Other Devices by sublimed

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