GUDIDData
gudid Primary ID: TS2301

AVCOO (UDI TS2301)

Manufactured by ADP HEALTH LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AVCOO - Primary ID TS2301

Device Regulatory Overview

The AVCOO (Model/Catalog Number: TS2301) is a medical device manufactured by ADP HEALTH LIMITED. This product is indexed under FDA Product Code / Category Classification NUH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
TS2301
Product Code / EMDN
NUH
Device Name
1) TENSThe device is designed to be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities (arm), lower extremities (leg), abdomen and bottom due to strain from exercise or normal household work activities.2) EMSThe device is designed to be used to stimulate healthy muscles in order to improve and facilitate muscle performance.
Database Sync Date
2026-08-09 09:37:37

Full Regulatory Attributes

🔒 Token Gated
{
    "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 AVCOO?

The registered manufacturer of record for AVCOO is ADP HEALTH LIMITED.

What is the Primary UDI-DI identifier for AVCOO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TS2301.

What classification code is assigned to this device?

This device is registered under product classification code NUH.

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