Swift Skin and Wound (UDI S1)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Swift Skin and Wound (Model/Catalog Number: S1) is a medical device manufactured by Swift Medical Inc. This product is indexed under FDA Product Code / Category Classification FXN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S1
Product Code / EMDN: FXN
Device Name
Database Sync Date: 2026-08-09 09:50:05

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 Swift Skin and Wound?

The registered manufacturer of record for Swift Skin and Wound is Swift Medical Inc.

What is the Primary UDI-DI identifier for Swift Skin and Wound?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S1.

What classification code is assigned to this device?

This device is registered under product classification code FXN.

Similar Classification Devices (FXN)

Other Devices by Swift Medical Inc

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