BD Multi-Check

BD Multi-Check™ CD4 Low Control

Registry build 21.09.26
3manufacturers in China registered for this device type
6catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code JPK
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
B&E BIO-Technology Co., Ltd. Yantai Shandong Manufacturer 9

Record

Regulatory record for BD Multi-Check
Listed by Becton, Dickinson AND Company, United States
FDA product code JPK
Device type Mixture, Hematology Quality Control
Device class Class 2
Regulation 21 CFR 864.8625
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2017-10-25
Record revised 2026-03-13 (version 8)

Specifications

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

Catalogue Numbers

Catalogue numbers for BD Multi-Check
Catalogue number Size Status
349702 In distribution
349701 In distribution
349705 In distribution
349700 In distribution
349703 In distribution
349704 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Research and Diagnostic Systems Research AND Diagnostic Systems, Inc. 140
Liquichek Bio-Rad Laboratories Inc. 34
Para 4 Streck LLC 17
Drew Scientific Drew Scientific, Ltd. 15
CVA Streck LLC 9
Stat Profile Nova Biomedical Corporation 8
Coulter 5C Beckman Coulter, Inc. 8
Retic-Chex II Streck LLC 7
Cell-Chex Auto Streck LLC 6
Coulter 4C-ES Beckman Coulter, Inc. 5
Trinity Biotech Primus Corp. 4
Difftrol Horiba Instruments Incorporated 4

Showing 12 of 97. All products under Mixture, Hematology Quality Control

Recalls Naming This Product

1 recall names this product by its own identifier, the UDI on its label.

Recalls naming the identifiers of BD Multi-Check
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Becton, Dickinson and Company, BD Biosciences UDI-DI 2020-10-05 Class II Process control Recent product complaints showing an unexpected cell population exhibiting dim CD3 expression that may result in inaccurate results gating. 619 vials 2022-03-11

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