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