Pasv MS Kit

PASV MS Kit with Pressure Activated Safety Valve with 4.5F x 5cm Dilator

Registry build 21.09.26
5manufacturers in China registered for this device type
4catalogue numbers in this listing
10510(k) clearances naming this product code
40recalls 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 Pasv MS Kit
Listed by AngioDynamics, Inc., 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, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2024-10-18
Record revised 2025-02-06 (version 2)

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
Packaging Box of 5
Sizes Catheter gauge 3.5 to 6.5 Fr; length 5 cm

Catalogue Numbers

Catalogue numbers for Pasv MS Kit
Catalogue number Size Status
M001MS4K0 Catheter Gauge 4.5 Fr In distribution
M001MS5K0 Length 5 cm In distribution
M001MS6K0 Length 5 cm In distribution
M001MS3K0 Catheter Gauge 3.5 Fr In distribution

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
Turbo-Ject Cook Incorporated 94
Cook Spectrum Turbo-Ject Cook Incorporated 73
Vascu-Picc®and Midline Catheters Medical Components Inc 55
Synergy Health Line International Corporation 53

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
K142889 2015-01-27
K093406 2010-03-25
K072196 2007-08-27
K070613 2007-06-29
K070615 2007-05-04
K060887 2006-04-28
K041420 2004-07-26
K040446 2004-03-05
K031626 2003-06-19
K030415 2003-04-30

Recalls

40 of these are Class II. Class II means a temporary or reversible health consequence. 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
2020-05-04 Class II Process control Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020. 119723 eaches total 2023-08-23
2020-05-04 Class II Process control Certain AngioDynamics PICC Kits contain BD PosiFlush SF Saline Flush Syringes which were recalled by BD Medical on April 16, 2020. 119723 eaches total 2023-08-23
2018-10-16 Class II Under Investigation by firm specific lots of Xcela Power Injectable and BioFlo PICCs are labelled with incorrect expiration dates.
The labelled expiration date extends the shelf life of the product beyond the date supported by
validation testing. Although the product
Box of 4 units 2020-06-26
2018-10-16 Class II Under Investigation by firm Specific lots of Xcela Power Injectable and BioFlo PICCs are labelled with incorrect expiration dates. The labelled expiration date extends the shelf life of the product beyond the date supported by validation testing. Although the product Box of 1 Units 2020-06-26
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 11 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 15 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 2 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 132 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 246 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 20 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 6 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 12 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 7 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 17 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 13 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 200 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 17 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 298 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 2 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 50 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 79 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 2 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 7 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 81 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 3 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 12 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 7 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 1 box 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 20 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 5 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 11 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 58 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 27 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 7 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 36 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 99 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 104 boxes 2020-05-13
2018-05-10 Class II Material/Component Contamination A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens). 2 boxes 2020-05-13
2016-11-28 Class II Component design/selection Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV, BioFlo PICC with PASV and the BioFlo PICC, conducted this recall to the end user level based on information received from Greatbatch Medical, the manufacturer of the 4591 units in total 2019-06-12
2016-11-28 Class II Component design/selection Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV, BioFlo PICC with PASV and the BioFlo PICC, conducted this recall to the end user level based on information received from Greatbatch Medical, the manufacturer of the 4591 units in total 2019-06-12

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