eudamed_udi
Primary ID: 08806182202193
LAP-iX (UDI 08806182202193)
Manufactured by SEJONG MEDICAL Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LAP-iX - Primary ID 08806182202193
Device Regulatory Overview
The LAP-iX (Model/Catalog Number: SI-ED-02-01) is a medical device manufactured by SEJONG MEDICAL Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0201010302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SI-ED-02-01
- Product Code / EMDN
- K0201010302
- Device Name
- SI-ED-02-01
- Database Sync Date
- 2026-08-09 17:28:53
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of LAP-iX?
The registered manufacturer of record for LAP-iX is SEJONG MEDICAL Co., Ltd..
What is the Primary UDI-DI identifier for LAP-iX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806182202193.
What classification code is assigned to this device?
This device is registered under product classification code K0201010302.
Similar Classification Devices (K0201010302)
Other Devices by SEJONG MEDICAL Co., Ltd.
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