gudid Primary ID: XTAC

XTAC (UDI XTAC)

Manufactured by PRESERVATION SOLUTIONS INC

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The XTAC (Model/Catalog Number: XTAC) is a medical device manufactured by PRESERVATION SOLUTIONS INC. This product is indexed under FDA Product Code / Category Classification FTL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: XTAC
Product Code / EMDN: FTL
Device Name: For temporary bridging of fascial defects where primary closure is not possible, including but not limited to, abdominal compartment syndrome.
Database Sync Date: 2026-08-09 09:22:17

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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Frequently Asked Questions

Who is the primary manufacturer of XTAC?

The registered manufacturer of record for XTAC is PRESERVATION SOLUTIONS INC.

What is the Primary UDI-DI identifier for XTAC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XTAC.

What classification code is assigned to this device?

This device is registered under product classification code FTL.

Similar Classification Devices (FTL)

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