gudid
Primary ID: 03.75.594
MUSTmini Straght Rod (UDI 03.75.594)
Manufactured by Medacta International SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MUSTmini Straght Rod - Primary ID 03.75.594
Device Regulatory Overview
The MUSTmini Straght Rod (Model/Catalog Number: 03.75.594) 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
- 03.75.594
- Product Code / EMDN
- NKG
- Device Name
- MUST MINI Rod Ti 3.5 x 50 mm
- Database Sync Date
- 2026-08-09 09:03:23
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 Straght Rod?
The registered manufacturer of record for MUSTmini Straght Rod is Medacta International SA.
What is the Primary UDI-DI identifier for MUSTmini Straght Rod?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03.75.594.
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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