PRO-Picc® CT

5F X 55CM Dual LUMEN5F X 55CM DU PRO-Picc®ct W/Valve Technology Full Nursing Kittechn W/MAX Barrierw/MAX Barrier

Registry build 21.09.26
5manufacturers in China registered for this device type
157catalogue 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 PRO-Picc® CT
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
Record published 2026-01-15
Record revised 2021-02-19 (version 7)

Specifications

Specifications
MRI safety MR Conditional
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 3, box of 4, box of 10, box of 6, inner box
Distribution end date 2026-03-31

Catalogue Numbers

Catalogue numbers for PRO-Picc® CT
Catalogue number Size Status
MD17036205 In distribution
MD17034105 In distribution
MRCTP41010 In distribution
MRCTP41003 In distribution
MD17036305 In distribution
MD17036205 In distribution
MR17035205N In distribution
MD17035105 In distribution
MD17036301 In distribution
MD17035202 In distribution
MR17035206MBN In distribution
MR17036306N In distribution
MD17036302 In distribution
MR82035205 In distribution
MR17036306MB In distribution
MD17034101 In distribution
MD17036201 In distribution
MD17035101 In distribution
MR17033106MB In distribution
MD17036305 In distribution
MRCTP52001 In distribution
MR17034106MBN In distribution
MD17035205 In distribution
MR17036205 In distribution
MD17035105 In distribution
MR17035206MB In distribution
MD17035202 In distribution
MD17036301 In distribution
MD17034105 In distribution
MRCTP52010 In distribution
MD17035101 In distribution
MD17035102 In distribution
MD17034101 In distribution
MD17035102 In distribution
MD17036202 In distribution
MD17035201 In distribution
MD17035205 In distribution
MD17034102 In distribution
MD17036201 In distribution
MD17036202 In distribution
MD17034102 In distribution
MR17035206N In distribution
MR17035106MB In distribution
MD17035201 In distribution
MRCTP52002 In distribution
MD17036302 In distribution
MR17034106MB In distribution
MD17034101 In distribution
MD17036311 Withdrawn
MR82035105 Withdrawn
MR17035211 Withdrawn
MR17035101 Withdrawn
MR17033106 Withdrawn
MR17035101-PE Withdrawn
MR82035106MB Withdrawn
MRCTP63006 Withdrawn
MRCTP41017 Withdrawn
MD17034105 Withdrawn
MRCTV63010 Withdrawn
MR82035202 Withdrawn
MR17034101 Withdrawn
MRCTP31026 Withdrawn
MR17036201 Withdrawn
MD17034102 Withdrawn
MR82034101 Withdrawn
MR17035201 Withdrawn
MRCTP63018 Withdrawn
MRCTP41007 Withdrawn
MR17033100 Withdrawn
MR82036301 Withdrawn
MR82036306MB Withdrawn
FVCT5D Withdrawn
MRCTP41028 Withdrawn
MRCTP63010 Withdrawn
MRCTP41010 Withdrawn
MRCTV52010 Withdrawn
MR17035206MB Withdrawn
MR82036302 Withdrawn
MRCTP52018NT Withdrawn
MR82035100 Withdrawn
MR17033105 Withdrawn
MR17035222 Withdrawn
MRCTP52028 Withdrawn
MRCTP52014 Withdrawn
MR17036202 Withdrawn
MR82035201 Withdrawn
MR82036306 Withdrawn
MD17036305 Withdrawn
MR17035206 Withdrawn
MRCTP52006 Withdrawn
MRCTP52008 Withdrawn
MRCTP51017 Withdrawn
MR17036306 Withdrawn
MR17034111 Withdrawn
MD17035211 Withdrawn
MRCTV41010 Withdrawn
MRCTP52005 Withdrawn
MR82035101 Withdrawn
MR17036305 Withdrawn
MR17033106 Withdrawn
MR17034106 Withdrawn
MR17035201-IL Withdrawn
MRCTP52029 Withdrawn
MR82035222 Withdrawn
MRCTP41014 Withdrawn
MR17035105 Withdrawn
MR17035102 Withdrawn
MR82034106MB Withdrawn
MRCTP63007 Withdrawn
MR17033101 Withdrawn
MR82036300 Withdrawn
MR82034102 Withdrawn
MR17035106 Withdrawn
MR82035206 Withdrawn
MR17034102 Withdrawn
MR17035205 Withdrawn
MD17036205 Withdrawn
MRCTP52013 Withdrawn
MRCTP63008 Withdrawn
MD17035111 Withdrawn
MRCTV52010 Withdrawn
MRCTP41001 Withdrawn
MRCTP51028 Withdrawn
MR17034100 Withdrawn
MR17035200 Withdrawn
MD17034111 Withdrawn
MR17035202 Withdrawn
MR17036302 Withdrawn
MR17033106MB Withdrawn
MR82034100 Withdrawn
MR17034106N Withdrawn
MRCTP41005 Withdrawn
MRCTP52005 Withdrawn
MRCTV41010 Withdrawn
MR17034105 Withdrawn
MRCTP52016 Withdrawn
MRCTP52017 Withdrawn
MD17036301 Withdrawn
MR17035206 Withdrawn
MR17036322 Withdrawn
MRCTP41029 Withdrawn
MRCTP52007 Withdrawn
MR17035111 Withdrawn
MR17036311 Withdrawn
MR82034106 Withdrawn
MRCTP52010 Withdrawn
MRCTP41029 Withdrawn
MRCTP52029 Withdrawn
MR82035206MB Withdrawn
MR82035102 Withdrawn
MR82034105 Withdrawn
MR17036301 Withdrawn
MRCTP63025 Withdrawn
CT5D800 Withdrawn
MR17033102 Withdrawn
MR82035200 Withdrawn
MD17036321 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
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
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