ABX Pentra Standard 1

Catalogue number 1220001717, listed by Horiba ABX SAS, France, under Calibrator, Multi-Analyte Mixture. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Jilin (1), Guangdong (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code JIX
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19

Record

Regulatory record for ABX Pentra Standard 1
Listed by Horiba ABX SAS, France
FDA product code JIX
Device type Calibrator, Multi-Analyte Mixture
Device class Class 2
Regulation 21 CFR 862.1150
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K052007
Record published 2016-08-16
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Label carries lot or batch number, expiry date

Catalogue Numbers

Catalogue numbers for ABX Pentra Standard 1
Catalogue number Size Status
1220001717 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Stat Profile Nova Biomedical Corporation 54
BioPlex 2200 Bio-Rad Laboratories Inc. 32
Plasma Calibrator Set Chromsystems Instruments & Chemicals Gmbh 22
Phoenix Diagnostics Phoenix Diagnostics, Inc. 20
Nova Nova Biomedical Corporation 15
Plasma Calibration Standard Chromsystems Instruments & Chemicals Gmbh 15
Phoenix Diagnostics, Inc. Phoenix Diagnostics, Inc. 15
Architect Abbott Laboratories 11
Alinity Abbott Medical 10
Synchron Beckman Coulter, Inc. 9
Architect Abbott Medical 9
Urine Calibration Standard Chromsystems Instruments & Chemicals Gmbh 8

Showing 12 of 229. All products under Calibrator, Multi-Analyte Mixture

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K071779 2008-03-05

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