AirLife (UDI 001904A)
Manufactured by Carefusion Corporation
Device Regulatory Overview
The AirLife (Model/Catalog Number: 001904A) is a medical device manufactured by Carefusion Corporation. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 001904A
- Product Code / EMDN
- BWF
- Device Name
- Airlife™ Volumetric Incentive Spirometer, 2500 ml
- Database Sync Date
- 2026-08-09 09:28:44
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?
The registered manufacturer of record for AirLife is Carefusion Corporation.
What is the Primary UDI-DI identifier for AirLife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 001904A.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by Carefusion Corporation
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