gudid
Primary ID: 04.01.10.1190
Shoulder System Instrument (UDI 04.01.10.1190)
Manufactured by Medacta International SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Shoulder System Instrument - Primary ID 04.01.10.1190
Device Regulatory Overview
The Shoulder System Instrument (Model/Catalog Number: 04.01.10.1190) is a medical device manufactured by Medacta International SA. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04.01.10.1190
- Product Code / EMDN
- LXH
- Device Name
- Trial hum. rev. constrained liner 32/+0 - SMALL
- Database Sync Date
- 2026-08-09 09:03:14
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 Shoulder System Instrument?
The registered manufacturer of record for Shoulder System Instrument is Medacta International SA.
What is the Primary UDI-DI identifier for Shoulder System Instrument?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04.01.10.1190.
What classification code is assigned to this device?
This device is registered under product classification code LXH.
Similar Classification Devices (LXH)
Other Devices by Medacta International SA
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