Cellpack-S

Concentrated diluent for use in hematology analyzers

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Shandong (3), Guangdong (1), Shanghai (1).

Chinese manufacturers registered for FDA product code GIF
Manufacturer City Province Registered as Device types
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Infitek Co., Ltd. Shanghai Shanghai Manufacturer 49
Labpeak Co., Ltd. Jinan Shandong Manufacturer 43
Scitek Global Co., Ltd. Jinan Shandong Manufacturer 43
B&E BIO-Technology Co., Ltd. Yantai Shandong Manufacturer 9

Record

Regulatory record for Cellpack-S
Listed by Sysmex Corporation, Japan
FDA product code GIF
Device type Diluent, Blood Cell
Device class Class 1
Regulation 21 CFR 864.8200
Establishment Manufacturer, Exporter
Premarket notification Exempt
Record published 2022-11-04
Record revised 2023-06-02 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 35 °C
Sizes Total volume 20 l

Catalogue Numbers

Catalogue numbers for Cellpack-S
Catalogue number Size Status
CPK-301A Total Volume 20 l In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Cell-DYN Abbott Laboratories 7
Cardinal Health Cardinal Health 200, LLC 5
Cellpack Sysmex Corporation 4
Cellpack DST Sysmex Corporation 4
Drew Scientific Drew Scientific, Ltd. 3
Atellica IM Multi-Diluent 1 Siemens Healthcare Diagnostics Inc 3
Cellpack DCL Sysmex Corporation 3
SP Cardinal Health 200, LLC 3
Needle Holder Koros U.S.A., Inc. 3
Advia Centaur® Multi-Diluent 1 Siemens Healthcare Diagnostics Inc 3
UF II Pack-SED Sysmex Corporation 2
Cellsheath Sysmex Corporation 2

Showing 12 of 88. All products under Diluent, Blood Cell

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K790028 1979-02-15

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