XINKANG (UDI 06972992540151)
Manufactured by JIANGSU XINKANG MEDICAL INSTRUMENT CO.LTD.
Device Regulatory Overview
The XINKANG (Model/Catalog Number: 1200) is a medical device manufactured by JIANGSU XINKANG MEDICAL INSTRUMENT CO.LTD.. This product is indexed under FDA Product Code / Category Classification W02069003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1200
- Product Code / EMDN
- W02069003
- Device Name
- Centrifuge
- Database Sync Date
- 2026-08-09 16:30:04
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 XINKANG?
The registered manufacturer of record for XINKANG is JIANGSU XINKANG MEDICAL INSTRUMENT CO.LTD..
What is the Primary UDI-DI identifier for XINKANG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06972992540151.
What classification code is assigned to this device?
This device is registered under product classification code W02069003.
Similar Classification Devices (W02069003)
Other Devices by JIANGSU XINKANG MEDICAL INSTRUMENT CO.LTD.
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