Vascu-Picc®

2.6F X 20CM Dual LUMEN2.6F X 20C VASCU-PICC®W/3F Tearaway Introducer Setintroducer SET

Registry build 21.09.26
5manufacturers in China registered for this device type
135catalogue numbers in this listing
9510(k) clearances naming this product code
5recalls 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 Vascu-Picc®
Listed by Medical Components 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, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2016-03-19
Record revised 2021-02-19 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Box of 5, box of 10, box of 3, box of 4
Distribution end date 2024-10-02

Catalogue Numbers

Catalogue numbers for Vascu-Picc®
Catalogue number Size Status
MD170126224S In distribution
MD170111024S In distribution
MRVSP42022 In distribution
MD170126024S In distribution
MD17011101 In distribution
MD17012601 In distribution
MRVSP42012 In distribution
MRVSP41012 In distribution
MR17012601 In distribution
MD17022621 In distribution
MD17012600 In distribution
MD170126224S In distribution
MRVSP1.9112 In distribution
MD17021101 In distribution
MD170111224S In distribution
VP1.9S20-NS In distribution
MRVSP52012 In distribution
MRVSP41013 In distribution
MD17012621 In distribution
MD17011121 In distribution
MD17011101 In distribution
MD17011121 In distribution
MR81015106MB In distribution
MR17015206N In distribution
MD170111224S In distribution
MR17011101 In distribution
MD17021121 In distribution
MD17012601 In distribution
VP1.9S20-NS In distribution
MR81015206MB In distribution
MR17014106MB In distribution
MD17022601 In distribution
MRVSP26001 In distribution
MD17022601 In distribution
MD170126024S In distribution
MD17012601 In distribution
MRVSP41022 In distribution
MRVSP19001 In distribution
MRVSP52016 In distribution
VP1.9S50-NS In distribution
MD17012621 In distribution
MD17022621 In distribution
MRVSP1.9122 In distribution
VP1.9S50-NS In distribution
MD17021121 In distribution
MD17021101 In distribution
MR17011101 In distribution
MRVSP52007 In distribution
MD17011100 In distribution
MR17014106N In distribution
MD17012621 In distribution
MD170111024S In distribution
MR17022621 Withdrawn
MR17014105 Withdrawn
MR17012600 Withdrawn
MR17014205 Withdrawn
MR17015102 Withdrawn
MR17013105 Withdrawn
MR17015101 Withdrawn
MD17011121 Withdrawn
VP3S-2C Withdrawn
MR17012608 Withdrawn
MR82013101 Withdrawn
MR82013106 Withdrawn
MR17021101 Withdrawn
MR17015301 Withdrawn
MRVSP41012 Withdrawn
MR170126024S Withdrawn
MR82014100 Withdrawn
MR17013106 Withdrawn
MR17015106 Withdrawn
MRVSP41015 Withdrawn
MR17011100 Withdrawn
MR17014100 Withdrawn
MR82014206 Withdrawn
MRVSP41023 Withdrawn
MR17013100 Withdrawn
MR17015206MB Withdrawn
MR81015306MB Withdrawn
MR17011121 Withdrawn
MR82015206 Withdrawn
MRVSP19001 Withdrawn
MR82014205 Withdrawn
MR82014106 Withdrawn
MR17012621 Withdrawn
MR17014206 Withdrawn
MR82014102 Withdrawn
MR170126224S Withdrawn
MR170111224S Withdrawn
MR17014106 Withdrawn
MR17022601 Withdrawn
MR82015201 Withdrawn
MR17016200 Withdrawn
MR17015206 Withdrawn
MR82014106MB Withdrawn
MR17014102 Withdrawn
VP4D-C Withdrawn
MR17014201 Withdrawn
MR82014101 Withdrawn
MR17015205 Withdrawn
MR17015305 Withdrawn
QACV5D Withdrawn
MR17015200 Withdrawn
MD17012600 Withdrawn
MR17015105 Withdrawn
MR170111024S Withdrawn
MR82013105 Withdrawn
MR82015206MB Withdrawn
MR82014200 Withdrawn
MR17012621-PE Withdrawn
MRVSP26001 Withdrawn
MR82014201 Withdrawn
MR82013100 Withdrawn
MR17014101 Withdrawn
MR17013101 Withdrawn
MR82015200 Withdrawn
MR17012601-PE Withdrawn
MRVSP42013 Withdrawn
MR17015201 Withdrawn
MRVSP42013 Withdrawn
MR17014200 Withdrawn
MR82015202 Withdrawn
VP5D-C Withdrawn
MR17015302 Withdrawn
MR82015205 Withdrawn
MR17015306MB Withdrawn
MD17011100 Withdrawn
MR17015202 Withdrawn
MD17011101 Withdrawn
MR82014105 Withdrawn
VP4S-C Withdrawn
MRVSP52012 Withdrawn
MR17012628 Withdrawn
MR17021121 Withdrawn
MR17016201 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
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
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
K141633 2014-09-29
K131687 2013-08-16
K123617 2013-05-15
K122423 2012-12-12
K121094 2012-06-06
K120980 2012-05-02
K120981 2012-05-02
K003682 2001-01-26
K983412 1998-12-10

Recalls

2 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
2018-10-01 Class II Software Manufacturing/Software Deployment When the iPad is updated with Apple
iOS software version 12, the C3 application malfunctions. Upon launching a new procedure, the ECG waves
do not appear on the screen, in surface or internal mode. If the C3 application is not operating pro
24 2020-10-01
2012-12-13 Class II Nonconforming Material/Component The affected product was packaged with the incorrect introducer needle. The kit label indicates a “safety” needle is included; the kits were packaged with a non-safety needle. 785 2013-07-31
2008-04-11 Not classified Mixed-up of materials/components kit contains incorrect component 250 units 2008-10-28
2005-09-15 Not classified Other The product is labelled as containing a 4F catheter when the trays/kits actually contain a 5F catheter. The catheters will not fit into the sheath-dilator that was included in the tray.

mislabeled as 4F

10 units 2005-11-22
2005-09-15 Not classified Other The product is labelled as containing a 4F catheter when the trays/kits actually contain a 5F catheter. The catheters will not fit into the sheath-dilator that was included in the tray.

mislabeled as 4F

88 units 2005-11-22

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