Atellica CH Ucfp

Atellica CH UCFP Reagent

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
6recalls on this code

Who Else Makes It

Concentrated in Zhejiang (1), Jilin (1), Shandong (1).

Chinese manufacturers registered for FDA product code CEK
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70

Record

Regulatory record for Atellica CH Ucfp
Listed by Siemens Healthcare Diagnostics Inc, United States
FDA product code CEK
Device type Biuret (Colorimetric), Total Protein
Device class Class 2
Regulation 21 CFR 862.1635
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2020-03-09
Record revised 2023-09-13 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 8 °C

Catalogue Numbers

Catalogue numbers for Atellica CH Ucfp
Catalogue number Size Per pack Status
11097543 4 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Biobase Biobase Biodustry(Shandong)Co., Ltd. 17
Synermed® Infrared Laboratory Systems LLC 10
JAS Diagnostics Drew Scientific, Ltd. 6
Pointe Scientific, Inc. Horiba Instruments Incorporated 5
AU Beckman Coulter, Inc. 5
Pointe Scientific, Inc. Total Protein Horiba Instruments Incorporated 5
Synchron Beckman Coulter, Inc. 3
Total Protein 2 (TP 2) Randox Laboratories Limited 3
Total Protein Roche Diagnostics Gmbh 3
Alinity Abbott Ireland 2
Pointe Total Protein Reagent Horiba Instruments Incorporated 2
Vitros Ortho-Clinical Diagnostics, Inc. 2

Showing 12 of 61. All products under Biuret (Colorimetric), Total Protein

Recalls Naming This Product

2 recalls name this product by its own identifiers, the UDI on its label.

Recalls naming the identifiers of Atellica CH Ucfp
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Siemens Healthcare Diagnostics Inc UDI-DI 2025-08-11 Class II Under Investigation by firm Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results. 11,811 units
Siemens Healthcare Diagnostics Inc UDI-DI 2024-07-29 Class II Under Investigation by firm The potential for biased quality control (QC) and
patient results when using Atellica CH UCFP lot 130414 and ADVIA Chemistry UCFP lot
140 reagents.
1,164 units (229 US, 935 OUS)

Recalls

4 of these are Class II. Class II means a temporary or reversible health consequence. 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
2024-07-29 Class II Under Investigation by firm The potential for biased quality control (QC) and
patient results when using Atellica CH UCFP lot 130414 and ADVIA Chemistry UCFP lot
140 reagents.
143 units (17 US, 126 OUS)
2023-01-27 Class II Under Investigation by firm Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP), Triglycerides (Trig), and Triglycerides_2 (Trig_2) Impacting Magnesium (Mg) Results 13071 units
2021-09-20 Class II Software design The firm has confirmed the potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely depressed Enzymatic Hemoglobin A1c results may affect cons 246 (US); 689 (OUS)
2021-09-20 Class II Software design The firm has confirmed the potential for Atellica CH Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Hemoglobin A1c (A1c_E and A1c_EM) results. Falsely depressed Enzymatic Hemoglobin A1c results may affect consider 1402 (US); 2941 (OUS)

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