GUDIDData
gudid Primary ID: A-4851.24TP

APTUS (UDI A-4851.24TP)

Manufactured by Medartis AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for APTUS - Primary ID A-4851.24TP

Device Regulatory Overview

The APTUS (Model/Catalog Number: A-4851.24TP) 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.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2361-2026 View Full Alert →

Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1549-2026 View Full Alert →

Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. P...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1550-2026 View Full Alert →

Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. P...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
A-4851.24TP
Product Code / EMDN
HRS
Device Name
Template for plate A-4851.24
Database Sync Date
2026-08-09 09:03:25

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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-4851.24TP.

What classification code is assigned to this device?

This device is registered under product classification code HRS.

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