eudamed_udi
Primary ID: 04719961405620
KP High Binder (UDI 04719961405620)
Manufactured by e-life International Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KP High Binder - Primary ID 04719961405620
Device Regulatory Overview
The KP High Binder (Model/Catalog Number: ACGKP01(M/UNI/Beige)) is a medical device manufactured by e-life International Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACGKP01(M/UNI/Beige)
- Product Code / EMDN
- M030499
- Device Name
- TRUNK COMPRESSION GARMENTS
- Database Sync Date
- 2026-08-09 16:29:38
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 KP High Binder?
The registered manufacturer of record for KP High Binder is e-life International Co., Ltd..
What is the Primary UDI-DI identifier for KP High Binder?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719961405620.
What classification code is assigned to this device?
This device is registered under product classification code M030499.
Similar Classification Devices (M030499)
Other Devices by e-life International Co., Ltd.
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