eudamed_udi
Primary ID: 04714123021274
Optical Trocar (UDI 04714123021274)
Manufactured by Lagis Enterprise Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Optical Trocar - Primary ID 04714123021274
Device Regulatory Overview
The Optical Trocar (Model/Catalog Number: TRO-08V2) is a medical device manufactured by Lagis Enterprise Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TRO-08V2
- Product Code / EMDN
- K01010103
- Device Name
- Trocar
- Database Sync Date
- 2026-08-09 16:29:31
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 Optical Trocar?
The registered manufacturer of record for Optical Trocar is Lagis Enterprise Co., Ltd..
What is the Primary UDI-DI identifier for Optical Trocar?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04714123021274.
What classification code is assigned to this device?
This device is registered under product classification code K01010103.
Similar Classification Devices (K01010103)
Other Devices by Lagis Enterprise Co., Ltd.
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