CIKOS PULSONIC ULTRASOUND AND ECG GEL 250ml (UDI 08682560954751)
Manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The CIKOS PULSONIC ULTRASOUND AND ECG GEL 250ml (Model/Catalog Number: 78400) is a medical device manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification Z11040185 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 78400
- Product Code / EMDN
- Z11040185
- Device Name
- Cikos PULSONIC
- Database Sync Date
- 2026-08-09 17:41:53
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 CIKOS PULSONIC ULTRASOUND AND ECG GEL 250ml?
The registered manufacturer of record for CIKOS PULSONIC ULTRASOUND AND ECG GEL 250ml is KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for CIKOS PULSONIC ULTRASOUND AND ECG GEL 250ml?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682560954751.
What classification code is assigned to this device?
This device is registered under product classification code Z11040185.
Similar Classification Devices (Z11040185)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint