Reusable Soft SpO2 Sensor (UDI 08698870323095)
Manufactured by METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ
Device Regulatory Overview
The Reusable Soft SpO2 Sensor (Model/Catalog Number: FMT-RPS/NVM) is a medical device manufactured by METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification C900301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FMT-RPS/NVM
- Product Code / EMDN
- C900301
- Device Name
- Non-Sterile Pulse Oximetry (SpO2) Sensor
- Database Sync Date
- 2026-08-09 16:28:51
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 Reusable Soft SpO2 Sensor?
The registered manufacturer of record for Reusable Soft SpO2 Sensor is METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Reusable Soft SpO2 Sensor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698870323095.
What classification code is assigned to this device?
This device is registered under product classification code C900301.
Similar Classification Devices (C900301)
Other Devices by METKO MEDİKAL VE TIBBİ CİHAZLAR DIŞ TİCARET SANAYİ ANONİM ŞİRKETİ
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