eudamed_udi
Primary ID: 59044737177914
DefiMax AED (UDI 59044737177914)
Manufactured by EMTEL Śliwa spółka komandytowa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DefiMax AED - Primary ID 59044737177914
Device Regulatory Overview
The DefiMax AED (Model/Catalog Number: DEFIMAXAED) is a medical device manufactured by EMTEL Śliwa spółka komandytowa. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DEFIMAXAED
- Product Code / EMDN
- Z12030501
- Device Name
- DefiMax AED - semi-automatic defibrillator
- Database Sync Date
- 2026-08-09 17:02:44
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 DefiMax AED?
The registered manufacturer of record for DefiMax AED is EMTEL Śliwa spółka komandytowa.
What is the Primary UDI-DI identifier for DefiMax AED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 59044737177914.
What classification code is assigned to this device?
This device is registered under product classification code Z12030501.
Similar Classification Devices (Z12030501)
Other Devices by EMTEL Śliwa spółka komandytowa
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