eudamed_udi
Primary ID: 42518911029776
Explorer 130mm Hollow Handle 10mm (UDI 42518911029776)
Manufactured by AR Instrumed
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Explorer 130mm Hollow Handle 10mm - Primary ID 42518911029776
Device Regulatory Overview
The Explorer 130mm Hollow Handle 10mm (Model/Catalog Number: 102-130H) is a medical device manufactured by AR Instrumed. This product is indexed under FDA Product Code / Category Classification L159003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 102-130H
- Product Code / EMDN
- L159003
- Device Name
- Explorers
- Database Sync Date
- 2026-08-09 16:44:47
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 Explorer 130mm Hollow Handle 10mm?
The registered manufacturer of record for Explorer 130mm Hollow Handle 10mm is AR Instrumed.
What is the Primary UDI-DI identifier for Explorer 130mm Hollow Handle 10mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 42518911029776.
What classification code is assigned to this device?
This device is registered under product classification code L159003.
Similar Classification Devices (L159003)
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