WANCARE (UDI 08682560953501)
Manufactured by KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The WANCARE (Model/Catalog Number: KAFG31-5) 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
- KAFG31-5
- Product Code / EMDN
- Z11040185
- Device Name
- ULTRASOUND ECG GEL
- Database Sync Date
- 2026-08-09 18:37:11
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of WANCARE?
The registered manufacturer of record for WANCARE is KAF GRUP SAĞLIK HİZMETLERİ İNŞAAT SANAYİ VE TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for WANCARE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682560953501.
What classification code is assigned to this device?
This device is registered under product classification code Z11040185.
Similar Classification Devices (Z11040185)
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