gudid
Primary ID: 72740
High Range AED II (UDI 72740)
Manufactured by UTAK LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for High Range AED II - Primary ID 72740
Device Regulatory Overview
The High Range AED II (Model/Catalog Number: 72740) is a medical device manufactured by UTAK LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification DIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 72740
- Product Code / EMDN
- DIF
- Device Name
- HR AED II
- Database Sync Date
- 2026-08-09 09:06:27
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 High Range AED II?
The registered manufacturer of record for High Range AED II is UTAK LABORATORIES, INC..
What is the Primary UDI-DI identifier for High Range AED II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 72740.
What classification code is assigned to this device?
This device is registered under product classification code DIF.
Similar Classification Devices (DIF)
Other Devices by UTAK LABORATORIES, INC.
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