Humidias (UDI 08698863810083)
Manufactured by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
Device Regulatory Overview
The Humidias (Model/Catalog Number: 0083) 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 R060201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0083
- Product Code / EMDN
- R060201
- Device Name
- Humidifier Chamber
- Database Sync Date
- 2026-08-09 17:19:47
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 Humidias?
The registered manufacturer of record for Humidias is Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti..
What is the Primary UDI-DI identifier for Humidias?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698863810083.
What classification code is assigned to this device?
This device is registered under product classification code R060201.
Similar Classification Devices (R060201)
Other Devices by Foras Bilgisayar Elektronik Medikal San. ve Tic. Ltd. Şti.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint