RAPIDPoint® 500e Blood Gas System

The RAPIDPoint® 500e Blood Gas System is a compact, bench-top analyzer designed for in vitro diagnostic testing and issuitable for professional use in a point-of-care or central laboratory…

Registry build 21.09.26

The RAPIDPoint® 500e Blood Gas System is a compact, bench-top analyzer designed for in vitro diagnostic testing and issuitable for professional use in a point-of-care or central laboratory environment. This system measures the following: blood gases,electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples.Additionally, the RAPIDPoint 500e Blood Gas System measures pH in pleural fluid.

1manufacturer
1catalogue number

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code JFP
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56

Record

Regulatory record for RAPIDPoint® 500e Blood Gas System
Listed by Siemens Healthcare Diagnostics Inc, United States
FDA product code JFP
Device type Electrode, Ion Specific, Calcium
Device class Class 2
Regulation 21 CFR 862.1145
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K192240
Record published 2020-04-15
Record revised 2021-11-19 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Storage environment temperature 4 to 40 °C

Catalogue Numbers

Catalogue numbers for RAPIDPoint® 500e Blood Gas System
Catalogue number Size Status
11416751 In distribution

Same Product Code

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Showing 12 of 33. All products under Electrode, Ion Specific, Calcium

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of RAPIDPoint® 500e Blood Gas System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Siemens Healthcare Diagnostics Inc 510(k) number 2024-05-17 Class II Software Design Change Siemens Healthineers has identified an issue with the RAPIDPoint500e system software version 5.3. This issue affects how the sample source is identified at the LIS when using the capillary mode. With this software version, samples run in th 9 units US
Siemens Healthcare Diagnostics Inc 510(k) number 2023-09-26 Class II Under Investigation by firm There are potential drug interferences from Perhexiline Maleate or Atomoxetine Hydrochloride that may cause falsely elevated sodium results reported on the RAPIDPoint 500 and RAPIDPoint 500e Blood Gas Systems. The erroneous sodium levels wi 8,749 units
Siemens Healthcare Diagnostics Inc 510(k) number 2022-06-01 Class II Under Investigation by firm Discrepant (low bias) pO2 results, could be an incorrect diagnosis of hypoxemia and initiation of unnecessary or inappropriate respiratory support. 263 Boxes
Siemens Healthcare Diagnostics Inc 510(k) number 2020-05-27 Class II Software design The scanner is not confirming the integrity of read barcode data using the check-digit when reading Code 39 barcodes. 436 2021-01-12

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer