eudamed_udi
Primary ID: 08806182206337
Laport (UDI 08806182206337)
Manufactured by SEJONG MEDICAL Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Laport - Primary ID 08806182206337
Device Regulatory Overview
The Laport (Model/Catalog Number: N53-1210P) is a medical device manufactured by SEJONG MEDICAL Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- N53-1210P
- Product Code / EMDN
- K01010101
- Device Name
- Laport
- Database Sync Date
- 2026-08-09 16:28:51
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 Laport?
The registered manufacturer of record for Laport is SEJONG MEDICAL Co., Ltd..
What is the Primary UDI-DI identifier for Laport?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806182206337.
What classification code is assigned to this device?
This device is registered under product classification code K01010101.
Similar Classification Devices (K01010101)
Other Devices by SEJONG MEDICAL Co., Ltd.
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