eudamed_udi
Primary ID: 04714123020819
Insufflation Needle (UDI 04714123020819)
Manufactured by Lagis Enterprise Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Insufflation Needle - Primary ID 04714123020819
Device Regulatory Overview
The Insufflation Needle (Model/Catalog Number: IN-150) is a medical device manufactured by Lagis Enterprise Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IN-150
- Product Code / EMDN
- K0104
- Device Name
- Insufflation Needle
- Database Sync Date
- 2026-08-09 17:39:59
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 Insufflation Needle?
The registered manufacturer of record for Insufflation Needle is Lagis Enterprise Co., Ltd..
What is the Primary UDI-DI identifier for Insufflation Needle?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04714123020819.
What classification code is assigned to this device?
This device is registered under product classification code K0104.
Similar Classification Devices (K0104)
Other Devices by Lagis Enterprise Co., Ltd.
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