Nenni (UDI 08698863811752)
Manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
Device Regulatory Overview
The Nenni (Model/Catalog Number: 1752) 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 Z12030102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1752
- Product Code / EMDN
- Z12030102
- Device Name
- Breathing Machines
- Database Sync Date
- 2026-08-09 16:45:04
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 Nenni?
The registered manufacturer of record for Nenni is Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti..
What is the Primary UDI-DI identifier for Nenni?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698863811752.
What classification code is assigned to this device?
This device is registered under product classification code Z12030102.
Similar Classification Devices (Z12030102)
Other Devices by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
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