eudamed_udi
Primary ID: 03770022399440
Clark (UDI 03770022399440)
Manufactured by LIFEAZ SAS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Clark - Primary ID 03770022399440
Device Regulatory Overview
The Clark (Model/Catalog Number: LFZ00531) 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
- LFZ00531
- Product Code / EMDN
- Z12030503
- Device Name
- AED CLARK 4G HU PRO
- Database Sync Date
- 2026-08-09 16:28:54
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 Clark?
The registered manufacturer of record for Clark is LIFEAZ SAS.
What is the Primary UDI-DI identifier for Clark?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770022399440.
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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