eudamed_udi
Primary ID: 00842071132132
Removal Tool (UDI 00842071132132)
Manufactured by Applied Medical Technology, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Removal Tool - Primary ID 00842071132132
Device Regulatory Overview
The Removal Tool (Model/Catalog Number: R-L3033) is a medical device manufactured by Applied Medical Technology, Inc.. This product is indexed under FDA Product Code / Category Classification G020299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R-L3033
- Product Code / EMDN
- G020299
- Device Name
- Non-Balloon Removal Tool
- Database Sync Date
- 2026-08-09 16:46:05
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 Removal Tool?
The registered manufacturer of record for Removal Tool is Applied Medical Technology, Inc..
What is the Primary UDI-DI identifier for Removal Tool?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842071132132.
What classification code is assigned to this device?
This device is registered under product classification code G020299.
Similar Classification Devices (G020299)
Other Devices by Applied Medical Technology, Inc.
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