K3Pro XP-Line Multiunit (UDI EAGNMUXP4020102SET2)
Manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
Device Regulatory Overview
The K3Pro XP-Line Multiunit (Model/Catalog Number: MU.XP 402010/2.SET) is a medical device manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MU.XP 402010/2.SET
- Product Code / EMDN
- P01020101
- Device Name
- K3Pro XP MultiUnit 20° Ø 4,0 GH 1,0 for 2mm Platform - incl. carrier screw
- Database Sync Date
- 2026-08-09 16:28:47
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 K3Pro XP-Line Multiunit?
The registered manufacturer of record for K3Pro XP-Line Multiunit is Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG.
What is the Primary UDI-DI identifier for K3Pro XP-Line Multiunit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EAGNMUXP4020102SET2.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
Other Devices by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
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