gudid
Primary ID: 03.75.890
MUSTmini Occipital plate (UDI 03.75.890)
Manufactured by Medacta International SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MUSTmini Occipital plate - Primary ID 03.75.890
Device Regulatory Overview
The MUSTmini Occipital plate (Model/Catalog Number: 03.75.890) is a medical device manufactured by Medacta International SA. This product is indexed under FDA Product Code / Category Classification NKG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03.75.890
- Product Code / EMDN
- NKG
- Device Name
- MUST MINI Occipital plate X Shape 4mm rod Large 40-50mm
- Database Sync Date
- 2026-08-09 09:03:24
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 MUSTmini Occipital plate?
The registered manufacturer of record for MUSTmini Occipital plate is Medacta International SA.
What is the Primary UDI-DI identifier for MUSTmini Occipital plate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03.75.890.
What classification code is assigned to this device?
This device is registered under product classification code NKG.
Similar Classification Devices (NKG)
Other Devices by Medacta International SA
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