Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner (UDI 06976873690010)
Manufactured by Jiangsu KR Pharmetech Co., Ltd.
Device Regulatory Overview
The Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner (Model/Catalog Number: 06976873690010) is a medical device manufactured by Jiangsu KR Pharmetech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06976873690010
- Product Code / EMDN
- W02079099
- Device Name
- Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner
- Database Sync Date
- 2026-08-09 16:50:46
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 Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner?
The registered manufacturer of record for Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner is Jiangsu KR Pharmetech Co., Ltd..
What is the Primary UDI-DI identifier for Fluorescence & Bright-Field Multifunctional Digital Pathology Scanner?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976873690010.
What classification code is assigned to this device?
This device is registered under product classification code W02079099.
Similar Classification Devices (W02079099)
Other Devices by Jiangsu KR Pharmetech Co., Ltd.
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