eudamed_udi
Primary ID: 03770022399310
AED CLARK 4G UK PRO (UDI 03770022399310)
Manufactured by LIFEAZ SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AED CLARK 4G UK PRO - Primary ID 03770022399310
Device Regulatory Overview
The AED CLARK 4G UK PRO (Model/Catalog Number: LFZ00499) is a medical device manufactured by LIFEAZ SAS. This product is indexed under FDA Product Code / Category Classification Z12030503 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LFZ00499
- Product Code / EMDN
- Z12030503
- Device Name
- Clark
- Database Sync Date
- 2026-08-09 16:51:39
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 AED CLARK 4G UK PRO?
The registered manufacturer of record for AED CLARK 4G UK PRO is LIFEAZ SAS.
What is the Primary UDI-DI identifier for AED CLARK 4G UK PRO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770022399310.
What classification code is assigned to this device?
This device is registered under product classification code Z12030503.
Similar Classification Devices (Z12030503)
Other Devices by LIFEAZ SAS
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