eudamed_udi
Primary ID: 04714123023391
Laparoscopic Kit (UDI 04714123023391)
Manufactured by Lagis Enterprise Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Laparoscopic Kit - Primary ID 04714123023391
Device Regulatory Overview
The Laparoscopic Kit (Model/Catalog Number: LB-1101) is a medical device manufactured by Lagis Enterprise Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01020120 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LB-1101
- Product Code / EMDN
- K01020120
- Device Name
- Laparoscopic Kit-LB Kit
- Database Sync Date
- 2026-08-09 17:18:17
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 Laparoscopic Kit?
The registered manufacturer of record for Laparoscopic Kit is Lagis Enterprise Co., Ltd..
What is the Primary UDI-DI identifier for Laparoscopic Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04714123023391.
What classification code is assigned to this device?
This device is registered under product classification code K01020120.
Similar Classification Devices (K01020120)
Other Devices by Lagis Enterprise Co., Ltd.
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