iFuge UC02R (UDI 89080197330446)
Manufactured by Accumax Lab Devices Private Limited
Device Regulatory Overview
The iFuge UC02R (Model/Catalog Number: iFuge UC02R) is a medical device manufactured by Accumax Lab Devices Private Limited. This product is indexed under FDA Product Code / Category Classification W02069005 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- iFuge UC02R
- Product Code / EMDN
- W02069005
- Device Name
- Refrigerated Universal Centrifuge
- Database Sync Date
- 2026-08-09 16:29:38
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 iFuge UC02R?
The registered manufacturer of record for iFuge UC02R is Accumax Lab Devices Private Limited.
What is the Primary UDI-DI identifier for iFuge UC02R?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 89080197330446.
What classification code is assigned to this device?
This device is registered under product classification code W02069005.
Similar Classification Devices (W02069005)
Other Devices by Accumax Lab Devices Private Limited
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