gudid
Primary ID: 4500
AIM (UDI 4500)
Manufactured by VITALOGRAPH (IRELAND) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AIM - Primary ID 4500
Device Regulatory Overview
The AIM (Model/Catalog Number: 4500) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification BWF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4500
- Product Code / EMDN
- BWF
- Device Name
- Vitalograph AIM
- Database Sync Date
- 2026-08-09 09:22:51
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 AIM?
The registered manufacturer of record for AIM is VITALOGRAPH (IRELAND) LIMITED.
What is the Primary UDI-DI identifier for AIM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4500.
What classification code is assigned to this device?
This device is registered under product classification code BWF.
Similar Classification Devices (BWF)
Other Devices by VITALOGRAPH (IRELAND) LIMITED
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