Automated Hematology Analyzer Diluent (UDI 06970291980791)
Manufactured by MedicalSystem Biotechnology Co., Ltd.
Device Regulatory Overview
The Automated Hematology Analyzer Diluent (Model/Catalog Number: XQ9001Y) is a medical device manufactured by MedicalSystem Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0103010103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XQ9001Y
- Product Code / EMDN
- W0103010103
- Device Name
- Automated Hematology Analyzer Diluent
- Database Sync Date
- 2026-08-09 16:29:59
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 Automated Hematology Analyzer Diluent?
The registered manufacturer of record for Automated Hematology Analyzer Diluent is MedicalSystem Biotechnology Co., Ltd..
What is the Primary UDI-DI identifier for Automated Hematology Analyzer Diluent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970291980791.
What classification code is assigned to this device?
This device is registered under product classification code W0103010103.
Similar Classification Devices (W0103010103)
Other Devices by MedicalSystem Biotechnology Co., Ltd.
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