eudamed_udi
Primary ID: 06970658141018
CPR System (UDI 06970658141018)
Manufactured by Ambulanc (Shenzhen) Tech. Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CPR System - Primary ID 06970658141018
Device Regulatory Overview
The CPR System (Model/Catalog Number: 211A) is a medical device manufactured by Ambulanc (Shenzhen) Tech. Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z120304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 211A
- Product Code / EMDN
- Z120304
- Device Name
- Cardiopulmonary resuscitator (CPR system)
- Database Sync Date
- 2026-08-09 16:51:18
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 CPR System?
The registered manufacturer of record for CPR System is Ambulanc (Shenzhen) Tech. Co., Ltd..
What is the Primary UDI-DI identifier for CPR System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970658141018.
What classification code is assigned to this device?
This device is registered under product classification code Z120304.
Similar Classification Devices (Z120304)
Other Devices by Ambulanc (Shenzhen) Tech. Co., Ltd.
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