eudamed_udi
Primary ID: 04560138481301
Extravasation Sensors LD (UDI 04560138481301)
Manufactured by Nemoto Kyorindo Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Extravasation Sensors LD - Primary ID 04560138481301
Device Regulatory Overview
The Extravasation Sensors LD (Model/Catalog Number: LD10110) is a medical device manufactured by Nemoto Kyorindo Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z11039080 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LD10110
- Product Code / EMDN
- Z11039080
- Device Name
- Extravasation Sensors LD
- Database Sync Date
- 2026-08-09 16:29:52
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 Extravasation Sensors LD?
The registered manufacturer of record for Extravasation Sensors LD is Nemoto Kyorindo Co., Ltd..
What is the Primary UDI-DI identifier for Extravasation Sensors LD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04560138481301.
What classification code is assigned to this device?
This device is registered under product classification code Z11039080.
Similar Classification Devices (Z11039080)
Other Devices by Nemoto Kyorindo Co., Ltd.
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