Viatrac

VIATRAC 14 Plus Peripheral Dilatation Catheter 4.0 mm x 15 mm x 135 cm

Registry build 21.09.26
5manufacturers in China registered for this device type
56catalogue numbers in this listing
7510(k) clearances naming this product code
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (3), Guangdong (2).

Chinese manufacturers registered for FDA product code LIT
Manufacturer City Province Registered as Device types
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for Viatrac
Listed by Abbott Vascular, United States
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-02-05
Record revised 2024-03-25 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep dry. Keep away from sunlight.

Catalogue Numbers

Catalogue numbers for Viatrac
Catalogue number Size Status
1008200-30 In distribution
1008189-15 In distribution
1008196-30 In distribution
1008198-15 In distribution
1008193-30 In distribution
1008195-15 In distribution
1008192-30 In distribution
1008195-40 In distribution
1008190-40 In distribution
1008199-40 In distribution
1008196-15 In distribution
1008192-40 In distribution
1008189-30 In distribution
1008195-20 In distribution
1008201-40 In distribution
1008199-20 In distribution
1008189-20 In distribution
1008202-30 In distribution
1008199-30 In distribution
1008200-40 In distribution
1008191-30 In distribution
1008192-15 In distribution
1008194-20 In distribution
1008189-40 In distribution
1008197-30 In distribution
1008200-20 In distribution
1008194-40 In distribution
1008201-15 In distribution
1008197-15 In distribution
1008202-40 In distribution
1008193-20 In distribution
1008198-40 In distribution
1008193-15 In distribution
1008197-20 In distribution
1008199-15 In distribution
1008195-30 In distribution
1008191-20 In distribution
1008194-15 In distribution
1008200-15 In distribution
1008191-15 In distribution
1008198-30 In distribution
1008197-40 In distribution
1008190-15 In distribution
1008190-30 In distribution
1008191-40 In distribution
1008201-20 In distribution
1008192-20 In distribution
1008194-30 In distribution
1008202-15 In distribution
1008193-40 In distribution
1008198-20 In distribution
1008190-20 In distribution
1008196-40 In distribution
1008201-30 In distribution
1008196-20 In distribution
1008202-20 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Parafleet SC 018 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 1,460
Jade Plus PTA Balloon Dilatation Catheter / Jade Plus 18 OTW OrbusNeich Medical (Shenzhen) Co., Ltd. 832
Jade PTA Balloon Dilatation Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 667
Parafleet SC 014 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 572
Minerva PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 504
Advocate Arravasc, Ltd. 441
Ultraverse® 035 PTA Dilatation Catheter Bard Peripheral Vascular, Inc. 361
Polux PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 359
Advance Cook Incorporated 355
Pacific™ Plus Medtronic, Inc. 347
EverCross™ ev3, Inc. 316
Achilles NC PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 297

Showing 12 of 167. All products under Catheter, Angioplasty, Peripheral, Transluminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K221057 2022-05-05
K151317 2015-07-06
K111899 2011-10-03
K102705 2010-12-07
K092286 2009-08-27
K081417 2008-06-04
K080925 2008-04-28

Recalls

1 of these is 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
2012-08-20 Class II Process design Abbott Vascular is recalling the Armada 35 and Armada 35 LL PTA Catheters because they have discovered that some devices may exhibit difficulty inflating and/or deflating. 61,799 units 2013-07-15
2009-05-06 Not classified Labeling mix-ups Abbott Vascular is initiating a recall on the Viatrac 14 Plus 5.0×15 mm Peripheral Dilation Catheter due to a mistake in labeling/packaging. 26 2012-03-30

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