GUDIDData
eudamed_udi Primary ID: 06951740550093

TENS Therapy Device (UDI 06951740550093)

Manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TENS Therapy Device - Primary ID 06951740550093

Device Regulatory Overview

The TENS Therapy Device (Model/Catalog Number: JPD-ES210) is a medical device manufactured by Shenzhen Jumper Medical Equipment Co.,Ltd. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
JPD-ES210
Product Code / EMDN
Z12062899
Device Name
TENS Therapy Device
Database Sync Date
2026-08-09 19:06:53

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 TENS Therapy Device?

The registered manufacturer of record for TENS Therapy Device is Shenzhen Jumper Medical Equipment Co.,Ltd.

What is the Primary UDI-DI identifier for TENS Therapy Device?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951740550093.

What classification code is assigned to this device?

This device is registered under product classification code Z12062899.

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