gudid
Primary ID: CP646003
EMI (UDI CP646003)
Manufactured by XIAMEN COMPOWER MEDICAL TECH. CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EMI - Primary ID CP646003
Device Regulatory Overview
The EMI (Model/Catalog Number: CP646003) is a medical device manufactured by XIAMEN COMPOWER MEDICAL TECH. CO., LTD. This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CP646003
- Product Code / EMDN
- CBP
- Device Name
- It contain one non-rebreathing valve. The non-rebreathing valve is a single-use, non-sterile device intended to be used with a ventilation mask to provide mouth-to-mask ventilation to health emergency victims requiring cardiopulmonary resuscitation (CPR) rescue techniques. It is intended for over-the counter-use.
- Database Sync Date
- 2026-08-09 09:05:30
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 EMI?
The registered manufacturer of record for EMI is XIAMEN COMPOWER MEDICAL TECH. CO., LTD.
What is the Primary UDI-DI identifier for EMI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CP646003.
What classification code is assigned to this device?
This device is registered under product classification code CBP.
Similar Classification Devices (CBP)
Other Devices by XIAMEN COMPOWER MEDICAL TECH. CO., LTD
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