ARGİ GRUP (UDI 08698753710875)
Manufactured by ARGİ GRUP SAĞLIK HİZMETLERİ TİCARET LİMİTED ŞİRKETİ
Device Regulatory Overview
The ARGİ GRUP (Model/Catalog Number: ARG11001PV) is a medical device manufactured by ARGİ GRUP SAĞLIK HİZMETLERİ TİCARET LİMİTED ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification N02010199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ARG11001PV
- Product Code / EMDN
- N02010199
- Device Name
- CSF External Lumbar Dranaige and ICP Monitoring System 4F
- Database Sync Date
- 2026-08-09 18:03:54
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 ARGİ GRUP?
The registered manufacturer of record for ARGİ GRUP is ARGİ GRUP SAĞLIK HİZMETLERİ TİCARET LİMİTED ŞİRKETİ.
What is the Primary UDI-DI identifier for ARGİ GRUP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698753710875.
What classification code is assigned to this device?
This device is registered under product classification code N02010199.
Similar Classification Devices (N02010199)
Other Devices by ARGİ GRUP SAĞLIK HİZMETLERİ TİCARET LİMİTED ŞİRKETİ
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