gudid
Primary ID: 3481AJ
Aerosure (UDI 3481AJ)
Manufactured by ACTEGY LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Aerosure - Primary ID 3481AJ
Device Regulatory Overview
The Aerosure (Model/Catalog Number: 3481AJ) is a medical device manufactured by ACTEGY LIMITED. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3481AJ
- Product Code / EMDN
- BWF
- Device Name
- Database Sync Date
- 2026-08-09 09:49:26
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 Aerosure?
The registered manufacturer of record for Aerosure is ACTEGY LIMITED.
What is the Primary UDI-DI identifier for Aerosure?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3481AJ.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by ACTEGY LIMITED
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