Advia® 360/560 Calibrator

Catalogue number 11170852, listed by Siemens Healthcare Diagnostics Inc, United States, under Calibrator For Hemoglobin And Hematocrit Measurement. 2 manufacturers in China are registered for this product code.

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
1recall

Who Else Makes It

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

Chinese manufacturers registered for FDA product code KRZ
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61

Record

Regulatory record for Advia® 360/560 Calibrator
Listed by Siemens Healthcare Diagnostics Inc, United States
FDA product code KRZ
Device type Calibrator For Hemoglobin And Hematocrit Measurement
Device class Class 2
Regulation 21 CFR 864.8165
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K955925
Record published 2016-09-24
Record revised 2021-11-18 (version 5)

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 Advia® 360/560 Calibrator
Catalogue number Size Status
11170852 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CDS Hematology Calibrator Clinical Diagnostic Solutions, Inc. 2
Variant II Hemoglobin A1c Bio-Rad Laboratories Inc. 2
Cal-Chex Streck LLC 2
Boule Cal Clinical Diagnostic Solutions, Inc. 1
Variant II Turbo Link Bio-Rad Laboratories Inc. 1
Architect Abbott Laboratories 1
Advia® 120/2120/2120i SETpoint Siemens Healthcare Diagnostics Inc 1
Cell-DYN Abbott Laboratories 1
Cfas HbA1c Roche Diagnostics Gmbh 1

Recalls

1 of these is 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
2025-06-04 Class II Under Investigation by firm Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems. 2,020 units

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