Vital Signs™ Manual Ventilation Components for ABS Bag Arm, Disposable, 0.9 m/36 in (UDI 10190752136137)
Manufactured by AirLife Finland Oy
Device Regulatory Overview
The Vital Signs™ Manual Ventilation Components for ABS Bag Arm, Disposable, 0.9 m/36 in (Model/Catalog Number: M1019517) is a medical device manufactured by AirLife Finland Oy. This product is indexed under FDA Product Code / Category Classification R03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M1019517
- Product Code / EMDN
- R03020101
- Device Name
- Vital Signs™ Anaesthesia Balloons
- Database Sync Date
- 2026-08-09 16:29:15
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 Vital Signs™ Manual Ventilation Components for ABS Bag Arm, Disposable, 0.9 m/36 in?
The registered manufacturer of record for Vital Signs™ Manual Ventilation Components for ABS Bag Arm, Disposable, 0.9 m/36 in is AirLife Finland Oy.
What is the Primary UDI-DI identifier for Vital Signs™ Manual Ventilation Components for ABS Bag Arm, Disposable, 0.9 m/36 in?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10190752136137.
What classification code is assigned to this device?
This device is registered under product classification code R03020101.
Similar Classification Devices (R03020101)
Other Devices by AirLife Finland Oy
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