Starrsed Control

Control blood for Starrsed Instruments and procedures

Registry build 21.09.26
4manufacturers in China registered for this device type
2catalogue numbers in this listing

Who Else Makes It

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

Chinese manufacturers registered for FDA product code GKB
Manufacturer City Province Registered as Device types
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70
Labpeak Co., Ltd. Jinan Shandong Manufacturer 43
Scitek Global Co., Ltd. Jinan Shandong Manufacturer 43
Shenzhen Yhlo Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 19

Record

Regulatory record for Starrsed Control
Listed by RR Mechatronics Manufacturing B.V., Netherlands
FDA product code GKB
Device type Device, Automated Sedimentation Rate
Device class Class 1
Regulation 21 CFR 864.5800
Establishment Manufacturer
Premarket notification Exempt
Record published 2022-12-05

Specifications

Specifications
MRI safety MR Safe
Sterilisation Liquid Chemical
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Packaging Blister pack of 6

Catalogue Numbers

Catalogue numbers for Starrsed Control
Catalogue number Size Status
QRR049001 In distribution
QRR049002 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Starrsed Mechatronics USA 16
Vision ESR Analyzer Shenzhen Yhlo Biotech Co., Ltd. 12
Excyte® ELITechGroup B.V. 4
Latex Controls Alifax SRL 4
Latex EQE (2 Test) Alifax SRL 3
Latex Calibrators Alifax SRL 2
Excyte® ESR Vacuum Tube, Carton ELITechGroup Inc 2
ESR-Auto Plus Streck LLC 2
Roller 20 Alifax SRL 2
Sediplus® S 2000 NX Sarstedt Aktiengesellschaft & Co.KG 2
Excyte 20 ELITechGroup Inc 2
Monosed® ESR Vacuum Tubes, Carton ELITechGroup Inc 2

Showing 12 of 47. All products under Device, Automated Sedimentation Rate

Recalls Naming This Product

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

Recalls naming the identifiers of Starrsed Control
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Mechatronics USA UDI-DI 2023-04-14 Class III Labeling Change Control QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28. The incorrectly labelled vial will upload the range for the Starrsed Control Level A and the instrument result will be flagged as out of range. 9306 units
Mechatronics USA UDI-DI 2023-04-14 Class III Labeling Change Control QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28. The incorrectly labelled vial will upload the range for the Starrsed Control Level A and the instrument result will be flagged as out of range. 10752 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