ClearCell® FX1 Unit

Catalogue number CBB-F011001-C, listed by Biolidics Limited, under Apparatus, Automated Blood Cell Diluting. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code GKH
Manufacturer City Province Registered as Device types
Suzhou Labyrinth Biotech Co., Ltd. Suzhou Jiangsu Manufacturer 2

Record

Regulatory record for ClearCell® FX1 Unit
Listed by Biolidics Limited
FDA product code GKH
Device type Apparatus, Automated Blood Cell Diluting
Device class Class 1
Regulation 21 CFR 864.5240
Premarket notification Exempt
Record published 2022-09-24

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries serial number

Catalogue Numbers

Catalogue numbers for ClearCell® FX1 Unit
Catalogue number Size Status
CBB-F011001-C In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CTR-S Ctcells, Inc. 1
Cell Isolator V2 Cytogen, Inc. 1
Ctcd Ctcells, Inc. 1
Smart Biopsy™ Cell Isolator Cytogen, Inc. 1
Smart Biopsy™ Isolation Kit Cytogen, Inc. 1
CTCeptor Ctcells, Inc. 1

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