eudamed_udi Primary ID: B786END2AA1000

EndoTENS Android app (UDI B786END2AA1000)

Manufactured by SUBLIMED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EndoTENS Android app (Model/Catalog Number: END2AA100) 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: END2AA100
Product Code / EMDN: Z120601
Device Name: actiTENS / actiTENS mini/ VitaliTENS / VitaliTENS mini
Database Sync Date: 2026-08-09 16:59:54

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 EndoTENS Android app?

The registered manufacturer of record for EndoTENS Android app is SUBLIMED.

What is the Primary UDI-DI identifier for EndoTENS Android app?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B786END2AA1000.

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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