BiNefes (UDI 08698863811684)
Manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
Device Regulatory Overview
The BiNefes (Model/Catalog Number: 1684) is a medical device manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification Z1203010504 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1684
- Product Code / EMDN
- Z1203010504
- Device Name
- Intensive Care Ventilator
- Database Sync Date
- 2026-08-09 16:49:22
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 BiNefes?
The registered manufacturer of record for BiNefes is Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti..
What is the Primary UDI-DI identifier for BiNefes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698863811684.
What classification code is assigned to this device?
This device is registered under product classification code Z1203010504.
Similar Classification Devices (Z1203010504)
Other Devices by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
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