gudid
Primary ID: 03.57.055
M.U.S.T. Pedicle Screw System (UDI 03.57.055)
Manufactured by Medacta International SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for M.U.S.T. Pedicle Screw System - Primary ID 03.57.055
Device Regulatory Overview
The M.U.S.T. Pedicle Screw System (Model/Catalog Number: 03.57.055) is a medical device manufactured by Medacta International SA. This product is indexed under FDA Product Code / Category Classification KWQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03.57.055
- Product Code / EMDN
- KWQ
- Device Name
- MUST LT 15mm SHORT - Pedicle Screw 8x60 Cann
- Database Sync Date
- 2026-08-09 09:03:18
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of M.U.S.T. Pedicle Screw System?
The registered manufacturer of record for M.U.S.T. Pedicle Screw System is Medacta International SA.
What is the Primary UDI-DI identifier for M.U.S.T. Pedicle Screw System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03.57.055.
What classification code is assigned to this device?
This device is registered under product classification code KWQ.
Similar Classification Devices (KWQ)
Other Devices by Medacta International SA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint