Aselsan Heartline (UDI 08682943410171)
Manufactured by RITIM GRUP TIBBI CIHAZLAR ELEKTRONIK SANAYI VE TICARET ANONIM SIRKETI
Device Regulatory Overview
The Aselsan Heartline (Model/Catalog Number: 6515-8444-0018) is a medical device manufactured by RITIM GRUP TIBBI CIHAZLAR ELEKTRONIK SANAYI VE TICARET ANONIM SIRKETI. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6515-8444-0018
- Product Code / EMDN
- Z12030501
- Device Name
- Aselsan Heartline AED Yarı Otomatik – Kapaklı – Ekranlı – RF Modül
- Database Sync Date
- 2026-08-09 16:47:23
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 Aselsan Heartline?
The registered manufacturer of record for Aselsan Heartline is RITIM GRUP TIBBI CIHAZLAR ELEKTRONIK SANAYI VE TICARET ANONIM SIRKETI.
What is the Primary UDI-DI identifier for Aselsan Heartline?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682943410171.
What classification code is assigned to this device?
This device is registered under product classification code Z12030501.
Similar Classification Devices (Z12030501)
Other Devices by RITIM GRUP TIBBI CIHAZLAR ELEKTRONIK SANAYI VE TICARET ANONIM SIRKETI
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint