Centrifuge (UDI 06972244261179)
Manufactured by Zhongke Meiling Cryogenics Company Limited.
Device Regulatory Overview
The Centrifuge (Model/Catalog Number: /) is a medical device manufactured by Zhongke Meiling Cryogenics Company Limited.. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- W02069003
- Device Name
- Centrifuge
- Database Sync Date
- 2026-08-09 16:28:58
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 Centrifuge?
The registered manufacturer of record for Centrifuge is Zhongke Meiling Cryogenics Company Limited..
What is the Primary UDI-DI identifier for Centrifuge?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972244261179.
What classification code is assigned to this device?
This device is registered under product classification code W02069003.
Similar Classification Devices (W02069003)
Other Devices by Zhongke Meiling Cryogenics Company Limited.
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