EasyRA Analyzer (ISE&LIS)

EasyRA Analyzer - ISE & LIS

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code JJY
Manufacturer City Province Registered as Device types
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19

Record

Regulatory record for EasyRA Analyzer (ISE&LIS)
Listed by Medica Corp., United States
FDA product code JJY
Device type Multi-Analyte Controls, All Kinds (Assayed)
Device class Class 1
Regulation 21 CFR 862.1660
Establishment Repacker / relabeller, Manufacturer
510(k) K070057
Record published 2019-02-14
Record revised 2022-09-16 (version 2)

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 25 °C

Catalogue Numbers

Catalogue numbers for EasyRA Analyzer (ISE&LIS)
Catalogue number Size Status
10340 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Liquichek Bio-Rad Laboratories Inc. 154
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InteliQ Bio-Rad Laboratories Inc. 50
Lyphochek Bio-Rad Laboratories Inc. 39
Stat Profile Nova Biomedical Corporation 38
i-STAT Abbott Point OF Care Inc. 24
Multichem AE Techno-Path Manufacturing Ltd. 20
Serum Control Chromsystems Instruments & Chemicals Gmbh 18
BioPlex 2200 Bio-Rad Laboratories Inc. 16
Nova Nova Biomedical Corporation 14
Plasma Control Chromsystems Instruments & Chemicals Gmbh 14
Multichem IA Speciality Techno-Path Manufacturing Ltd. 12

Showing 12 of 559. All products under Multi-Analyte Controls, All Kinds (Assayed)

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of EasyRA Analyzer (ISE&LIS)
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Medica Corp. 510(k) number 2010-03-29 Not classified Other Chemistry analyzers may report Calcium results below the sample’s actual concentration. Reported results may be ten to fifteen percent lower than expected sample results.

The defect is a shortened path length at specific cuvette positions

14,926 2011-06-07

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