AirLife™ Infant Skin Temperature Probe, Single Patient Use (Lullaby™, CarePlus™) (UDI 10190752181199)
Manufactured by AirLife Finland Oy
Device Regulatory Overview
The AirLife™ Infant Skin Temperature Probe, Single Patient Use (Lullaby™, CarePlus™) (Model/Catalog Number: 6600-0196-700) is a medical device manufactured by AirLife Finland Oy. This product is indexed under FDA Product Code / Category Classification V03010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6600-0196-700
- Product Code / EMDN
- V03010201
- Device Name
- AirLife™ Temperature monitoring
- Database Sync Date
- 2026-08-09 16:46:39
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 AirLife™ Infant Skin Temperature Probe, Single Patient Use (Lullaby™, CarePlus™)?
The registered manufacturer of record for AirLife™ Infant Skin Temperature Probe, Single Patient Use (Lullaby™, CarePlus™) is AirLife Finland Oy.
What is the Primary UDI-DI identifier for AirLife™ Infant Skin Temperature Probe, Single Patient Use (Lullaby™, CarePlus™)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10190752181199.
What classification code is assigned to this device?
This device is registered under product classification code V03010201.
Similar Classification Devices (V03010201)
Other Devices by AirLife Finland Oy
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