GUDIDData
pma Primary ID: P930027

IMMULITE/IMMULITE 2000 PSA (UDI P930027)

Manufactured by Siemens Healthcare Diagnostics, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IMMULITE/IMMULITE 2000 PSA - Primary ID P930027

Device Regulatory Overview

The IMMULITE/IMMULITE 2000 PSA (Model/Catalog Number: Unspecified) is a medical device manufactured by Siemens Healthcare Diagnostics, Inc.. This product is indexed under FDA Product Code / Category Classification MTF within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2703-2026 View Full Alert →

Atellica CH Enzymatic Hemoglobin A1c (A1c_E). Material Number: 11097536....

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ID: Z-2398-2026 View Full Alert →

Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay...

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ID: Z-1980-2026 View Full Alert →

Dimension Creatinine Flex reagent cartridge. Material Number: 10872079....

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Technical Specifications

Model Number
N/A
Product Code / EMDN
MTF
Device Name
Total, prostate specific antigen (noncomplexed & complexed) for detection of prostate cancer
Database Sync Date
2026-08-09 10:04:44

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of IMMULITE/IMMULITE 2000 PSA?

The registered manufacturer of record for IMMULITE/IMMULITE 2000 PSA is Siemens Healthcare Diagnostics, Inc..

What is the Primary UDI-DI identifier for IMMULITE/IMMULITE 2000 PSA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P930027.

What classification code is assigned to this device?

This device is registered under product classification code MTF.

Programmatic Export

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