BEOKA (UDI ACM-A1/Beoka/Black(XL)/Standard Edition)
Manufactured by SiChuan Qian Li Beoka Medical Technology Co., Ltd.
Device Regulatory Overview
The BEOKA (Model/Catalog Number: ACM-A1/Beoka/Black(XL)/Standard Edition) is a medical device manufactured by SiChuan Qian Li Beoka Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification IRP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACM-A1/Beoka/Black(XL)/Standard Edition
- Product Code / EMDN
- IRP
- Device Name
- The Air Compression Massager is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas.
- Database Sync Date
- 2026-08-09 09:05:26
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 BEOKA?
The registered manufacturer of record for BEOKA is SiChuan Qian Li Beoka Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for BEOKA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACM-A1/Beoka/Black(XL)/Standard Edition.
What classification code is assigned to this device?
This device is registered under product classification code IRP.
Similar Classification Devices (IRP)
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