Turbo-Ject

Turbo-Ject PICC Tray Power Injectable Polyurethane Peripherally Inserted Central Venous Catheter

Registry build 21.09.26
5manufacturers in China registered for this device type
94catalogue numbers in this listing
9510(k) clearances naming this product code
10recalls on this code

Who Else Makes It

Concentrated in Guangdong (3), Zhejiang (1), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LJS
Manufacturer City Province Registered as Device types
Hantech Medical Device Co., Ltd. Cixi Zhejiang Contract manufacturer 18
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Taijia Medical Electronics (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Chison Medical Technologies Co., Ltd. Wuxi Jiangsu Contract manufacturer 5
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6

Record

Regulatory record for Turbo-Ject
Listed by Cook Incorporated, United States
FDA product code LJS
Device type Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Device class Class 2
Regulation 21 CFR 880.5970
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-24
Record revised 2022-02-03 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in dark, dry, cool place.
Distribution end date 2022-02-02

Catalogue Numbers

Catalogue numbers for Turbo-Ject
Catalogue number Size Status
G49162 In distribution
G34512 In distribution
G23922 In distribution
G34525 In distribution
G03789 In distribution
G23930 In distribution
G23904 In distribution
G03778 In distribution
G49174 In distribution
G49171 In distribution
G23716 In distribution
G49163 In distribution
G34524 In distribution
G34520 In distribution
G23899 In distribution
G49168 In distribution
G49159 In distribution
G23920 In distribution
G49178 In distribution
G03776 In distribution
G23921 In distribution
G23906 In distribution
G49176 In distribution
G03787 In distribution
G34530 In distribution
G49177 In distribution
G49169 In distribution
G49164 In distribution
G34528 In distribution
G49165 In distribution
G23928 In distribution
G03786 In distribution
G49181 In distribution
G49160 In distribution
G49161 In distribution
G34527 In distribution
G49175 In distribution
G49170 In distribution
G23927 In distribution
G23919 In distribution
G34529 In distribution
G34532 In distribution
G49172 In distribution
G49173 In distribution
G49166 In distribution
G55882 In distribution
G49167 In distribution
G49180 In distribution
G23924 In distribution
G34523 In distribution
G34522 In distribution
G23929 In distribution
G23923 In distribution
G34526 In distribution
G23714 In distribution
G55885 In distribution
G34515 In distribution
G34531 In distribution
G55889 In distribution
G34516 Withdrawn
G34519 Withdrawn
G23903 Withdrawn
G03780 Withdrawn
G55883 Withdrawn
G56194 Withdrawn
G55888 Withdrawn
G03788 Withdrawn
G03785 Withdrawn
G23900 Withdrawn
G23905 Withdrawn
G03779 Withdrawn
G34518 Withdrawn
G23896 Withdrawn
G34521 Withdrawn
G23713 Withdrawn
G56199 Withdrawn
G55886 Withdrawn
G23717 Withdrawn
G34513 Withdrawn
G20061 Withdrawn
G23897 Withdrawn
G23902 Withdrawn
G23898 Withdrawn
G23901 Withdrawn
G23715 Withdrawn
G03777 Withdrawn
G55884 Withdrawn
G34511 Withdrawn
G56196 Withdrawn
G23712 Withdrawn
G55887 Withdrawn
G34517 Withdrawn
G03783 Withdrawn
G34514 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 1,548
BioFlo Navilyst Medical, Inc. 658
PowerPICC Bard Access Systems, Inc. 477
PowerPICC Solo Bard Access Systems, Inc. 333
PowerPICC Provena Bard Access Systems, Inc. 312
Xcela Navilyst Medical, Inc. 271
PRO-Picc® CT Medical Components Inc 157
Vascu-Picc® Medical Components Inc 135
Cook Spectrum Turbo-Ject Cook Incorporated 73
Vascu-Picc®and Midline Catheters Medical Components Inc 55
Synergy Health Line International Corporation 53
Vygon Vygon Corp. 50

Showing 12 of 194. All products under Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K171994 2018-02-22
K161496 2016-10-07
K133634 2013-12-23
K132885 2013-10-11
K132334 2013-08-16
K111244 2011-06-14
K072625 2007-12-13
K041849 2005-07-21
K851243 1986-03-14

Recalls

The FDA has not published a severity grade for these. 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 Closed
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21
2010-10-04 Not classified Nonconforming Material/Component Cook, Inc. is recalling Single, Double, Triple, and Five-Lumen Central Venous Catheter Trays AND Single and Double Lumen PICC Peripherally Inserted Central Venous Catheter Trays. These kits and trays contain 0.9% Sodium Chloride Injection 51,473 total kits/trays 2011-06-21

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