DIMENSIONS FPSA FLEX REAGENT CARTRIDGE (UDI P020027)
Manufactured by Siemens Healthcare Diagnostics
Device Regulatory Overview
The DIMENSIONS FPSA FLEX REAGENT CARTRIDGE (Model/Catalog Number: Unspecified) is a medical device manufactured by Siemens Healthcare Diagnostics. This product is indexed under FDA Product Code / Category Classification MTG within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- MTG
- Device Name
- Test, prostate specific antigen, free, (noncomplexed) to distinguish prostate cancer from benign conditions
- Database Sync Date
- 2026-08-09 10:04:45
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 DIMENSIONS FPSA FLEX REAGENT CARTRIDGE?
The registered manufacturer of record for DIMENSIONS FPSA FLEX REAGENT CARTRIDGE is Siemens Healthcare Diagnostics.
What is the Primary UDI-DI identifier for DIMENSIONS FPSA FLEX REAGENT CARTRIDGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P020027.
What classification code is assigned to this device?
This device is registered under product classification code MTG.
Similar Classification Devices (MTG)
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