BFT II Analyzer Dispo System (UDI 10446530)
Manufactured by Siemens Healthcare Diagnostics Products GmbH
Device Regulatory Overview
The BFT II Analyzer Dispo System (Model/Catalog Number: 10446530) is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10446530
- Product Code / EMDN
- JPA
- Device Name
- The cuvettes serve coagulation tests as a reaction vessel.
- Database Sync Date
- 2026-08-09 09:13:52
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 BFT II Analyzer Dispo System?
The registered manufacturer of record for BFT II Analyzer Dispo System is Siemens Healthcare Diagnostics Products GmbH.
What is the Primary UDI-DI identifier for BFT II Analyzer Dispo System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10446530.
What classification code is assigned to this device?
This device is registered under product classification code JPA.
Similar Classification Devices (JPA)
Other Devices by Siemens Healthcare Diagnostics Products GmbH
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