APTUS (UDI A-4750.124)
Manufactured by Medartis AG
Device Regulatory Overview
The APTUS (Model/Catalog Number: A-4750.124) is a medical device manufactured by Medartis AG. This product is indexed under FDA Product Code / Category Classification HRS within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- A-4750.124
- Product Code / EMDN
- HRS
- Device Name
- 2.5 TriLock Dist.Rad.FPL.Pl Volar Right
- Database Sync Date
- 2026-08-09 09:03:25
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 APTUS?
The registered manufacturer of record for APTUS is Medartis AG.
What is the Primary UDI-DI identifier for APTUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A-4750.124.
What classification code is assigned to this device?
This device is registered under product classification code HRS.
Similar Classification Devices (HRS)
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