Dr. Aktive (UDI A02-C-032-F)
Manufactured by Chengdu Cryo-push Medical Technology Co.,Ltd.
Device Regulatory Overview
The Dr. Aktive (Model/Catalog Number: A02-C-032-F) is a medical device manufactured by Chengdu Cryo-push 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
- A02-C-032-F
- Product Code / EMDN
- IRP
- Device Name
- Hot and Cold Compression System-Elbow cuff
- Database Sync Date
- 2026-08-09 09:06:39
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 Dr. Aktive?
The registered manufacturer of record for Dr. Aktive is Chengdu Cryo-push Medical Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Dr. Aktive?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A02-C-032-F.
What classification code is assigned to this device?
This device is registered under product classification code IRP.
Similar Classification Devices (IRP)
Other Devices by Chengdu Cryo-push Medical Technology Co.,Ltd.
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