eudamed_udi
Primary ID: 08806182217197
Lapbag (UDI 08806182217197)
Manufactured by SEJONG MEDICAL Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lapbag - Primary ID 08806182217197
Device Regulatory Overview
The Lapbag (Model/Catalog Number: B12-1208) is a medical device manufactured by SEJONG MEDICAL Co., Ltd.. This product is indexed under FDA Product Code / Category Classification S01010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B12-1208
- Product Code / EMDN
- S01010301
- Device Name
- Lapbag Non Metal Type
- Database Sync Date
- 2026-08-09 16:28:49
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 Lapbag?
The registered manufacturer of record for Lapbag is SEJONG MEDICAL Co., Ltd..
What is the Primary UDI-DI identifier for Lapbag?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08806182217197.
What classification code is assigned to this device?
This device is registered under product classification code S01010301.
Similar Classification Devices (S01010301)
Other Devices by SEJONG MEDICAL Co., Ltd.
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