gudid Primary ID: AK-0455/AP

Full Handle Backflush 23G Soft tip Active/Passive (UDI AK-0455/AP)

Manufactured by AKTIVE SRL

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Full Handle Backflush 23G Soft tip Active/Passive (Model/Catalog Number: AK-0455/AP) is a medical device manufactured by AKTIVE SRL. This product is indexed under FDA Product Code / Category Classification KYG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AK-0455/AP
Product Code / EMDN: KYG
Device Name: Full Handle Backflush 23G Soft tip Active/Passive
Database Sync Date: 2026-08-09 09:04:32

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 Full Handle Backflush 23G Soft tip Active/Passive?

The registered manufacturer of record for Full Handle Backflush 23G Soft tip Active/Passive is AKTIVE SRL.

What is the Primary UDI-DI identifier for Full Handle Backflush 23G Soft tip Active/Passive?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AK-0455/AP.

What classification code is assigned to this device?

This device is registered under product classification code KYG.

Similar Classification Devices (KYG)

Other Devices by AKTIVE SRL

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