eudamed_udi
Primary ID: 06974442401036
Acoresmed (UDI 06974442401036)
Manufactured by Acoresmed Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acoresmed - Primary ID 06974442401036
Device Regulatory Overview
The Acoresmed (Model/Catalog Number: A112) is a medical device manufactured by Acoresmed Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A112
- Product Code / EMDN
- Z12030501
- Device Name
- Automated external defibrillator
- Database Sync Date
- 2026-08-09 16:58:36
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 Acoresmed?
The registered manufacturer of record for Acoresmed is Acoresmed Co., Ltd..
What is the Primary UDI-DI identifier for Acoresmed?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974442401036.
What classification code is assigned to this device?
This device is registered under product classification code Z12030501.
Similar Classification Devices (Z12030501)
Other Devices by Acoresmed Co., Ltd.
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