gudid
Primary ID: CP-0400
AirLife (UDI CP-0400)
Manufactured by SUNMED, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AirLife - Primary ID CP-0400
Device Regulatory Overview
The AirLife (Model/Catalog Number: CP-0400) is a medical device manufactured by SUNMED, LLC. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CP-0400
- Product Code / EMDN
- JAY
- Device Name
- AirLife Large Tube Tackles
- 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 SUNMED, LLC.
What is the Primary UDI-DI identifier for AirLife?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CP-0400.
What classification code is assigned to this device?
This device is registered under product classification code JAY.
Similar Classification Devices (JAY)
Other Devices by SUNMED, LLC
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