GUDIDData
gudid Primary ID: AK-0466/APXL

Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm) (UDI AK-0466/APXL)

Manufactured by AKTIVE SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm) - Primary ID AK-0466/APXL

Device Regulatory Overview

The Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm) (Model/Catalog Number: AK-0466/APXL) 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-0466/APXL
Product Code / EMDN
KYG
Device Name
Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm)
Database Sync Date
2026-08-09 09:04:32

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm)?

The registered manufacturer of record for Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm) is AKTIVE SRL.

What is the Primary UDI-DI identifier for Full Handle Backflush 27G Brush tip Active/Passive (1,5 mm)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AK-0466/APXL.

What classification code is assigned to this device?

This device is registered under product classification code KYG.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint