Access Sensitive Estradiol

The Access Sensitive Estradiol assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of estradiol levels in human serum and plasma using the…

Registry build 21.09.26

The Access Sensitive Estradiol assay is a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of estradiol levels in human serum and plasma using the Access Immunoassay Systems.

5manufacturers in China registered for this device type
1catalogue number
2recalls on this code

Who Else Makes It

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

Chinese manufacturers registered for FDA product code CHP
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Shijiazhuang Hipro Biotechnology Co., Ltd. Shijiazhuang Hebei Manufacturer 22
Shenzhen Yhlo Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 19
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19
Beijing Hotgen Biotech Co., Ltd. Beijing Beijing Manufacturer 13

Record

Regulatory record for Access Sensitive Estradiol
Listed by Beckman Coulter, Inc., United States
FDA product code CHP
Device type Radioimmunoassay, Estradiol
Device class Class 1
Regulation 21 CFR 862.1260
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Premarket notification Exempt
Record published 2023-06-26

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Access Sensitive Estradiol
Catalogue number Size Status
B84493 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Salimetrics Salimetrics LLC. 5
MP Biomedicals LLC Mp Biomedicals, LLC 4
17beta-Estradiol Saliva Luminescence Immunoassay IBL International Gmbh 4
Elecsys Estradiol III Roche Diagnostics Gmbh 3
Alinity Abbott Ireland 3
Advia Centaur® eE2 Siemens Healthcare Diagnostics Inc 3
Architect Abbott Ireland 3
Atellica IM eE2 Siemens Healthcare Diagnostics Inc 3
Pantex Pantex 2
Estradiol Sensitive Elisa DRG Instruments Gesellschaft mit beschränkter Haftung 2
Salivary Estradiol Elisa DRG Instruments Gesellschaft mit beschränkter Haftung 2
Ultrasensitive Estradiol Elisa American Laboratory Products Company 2

Showing 12 of 58. All products under Radioimmunoassay, Estradiol

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2010-03-04 Not classified Other The recall was initiated after Beckman Coulter confirmed that three lots of Access Estradiol reagent (REF 33540) contains an incorrect raw material which may produce incorrect patient results. 20,209 units (5475 in US) 2012-05-07
2003-05-08 Not classified Other Short volume, resulting possibility of falsely elevated results. 1593 kits 2003-10-14

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