GUDIDData
gudid Primary ID: FA2C021CBUS0

Ninjo (UDI FA2C021CBUS0)

Manufactured by Arjohuntleigh AB

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ninjo - Primary ID FA2C021CBUS0

Device Regulatory Overview

The Ninjo (Model/Catalog Number: FA2C021CBUS0) is a medical device manufactured by Arjohuntleigh AB. This product is indexed under FDA Product Code / Category Classification FLH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FA2C021CBUS0
Product Code / EMDN
FLH
Device Name
Ninjo flusher disinfector, FD1615
Database Sync Date
2026-08-09 09:08:10

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 Ninjo?

The registered manufacturer of record for Ninjo is Arjohuntleigh AB.

What is the Primary UDI-DI identifier for Ninjo?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FA2C021CBUS0.

What classification code is assigned to this device?

This device is registered under product classification code FLH.

Programmatic Export

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

JSON API Endpoint