eudamed_udi
Primary ID: 08809261002899
REA (UDI 08809261002899)
Manufactured by TS Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REA - Primary ID 08809261002899
Device Regulatory Overview
The REA (Model/Catalog Number: 08809261002899) is a medical device manufactured by TS Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M03040299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 08809261002899
- Product Code / EMDN
- M03040299
- Device Name
- Kinesiology tape
- Database Sync Date
- 2026-08-09 16:46:23
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of REA?
The registered manufacturer of record for REA is TS Co., Ltd..
What is the Primary UDI-DI identifier for REA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809261002899.
What classification code is assigned to this device?
This device is registered under product classification code M03040299.
Similar Classification Devices (M03040299)
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