GUDIDData
eudamed_udi Primary ID: 06979191881023

Kinesiology Tape (UDI 06979191881023)

Manufactured by Nanjing 3H Medical Products Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kinesiology Tape - Primary ID 06979191881023

Device Regulatory Overview

The Kinesiology Tape (Model/Catalog Number: rule1) is a medical device manufactured by Nanjing 3H Medical Products Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification M030403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
rule1
Product Code / EMDN
M030403
Device Name
Kinesiology tape
Database Sync Date
2026-08-09 16:29:03

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 Kinesiology Tape?

The registered manufacturer of record for Kinesiology Tape is Nanjing 3H Medical Products Co.,Ltd..

What is the Primary UDI-DI identifier for Kinesiology Tape?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06979191881023.

What classification code is assigned to this device?

This device is registered under product classification code M030403.

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