OTW Takeru

OTW Takeru is an over-the-wire balloon catheter for dilating coronary artery or bypass graft stenosis. Its distal balloon inflates through an external inflation device connected to the…

Registry build 21.09.26

OTW Takeru is an over-the-wire balloon catheter for dilating coronary artery or bypass graft stenosis. Its distal balloon inflates through an external inflation device connected to the proximal manifold. A separate guidewire lumen runs along the catheter to a port on that manifold.

The catheter accepts a guidewire up to 0.014 inches and is compatible with 5 or 6 Fr guiding catheters. Nominal balloon diameters range from 1.5 to 5.0 mm, with working lengths from 6 to 30 mm. Catheter working length is 1,450 mm.

Listed Item

OTW TAKERU is a Percutaneous Transluminal Coronary Angioplasty (PTCA) Balloon Dilatation Catheter for coronary indications. OTW TAKERU is an over the wire (OTW) type and the maximum diameter of the compatible guidewire is 0.014 inches (0.36 mm).

Stent Expansion and Design

Balloon models from 2.0 to 5.0 mm are also indicated for expanding balloon-expandable stents after delivery. Radiopaque markers identify the balloon region, while the shaft includes hydrophilic coating and strain relief. The stent expansion indication does not extend to the smallest 1.5 mm balloon.

12manufacturers in China registered for this device type
66catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (4), Guangdong (3), Beijing (2).

Chinese manufacturers registered for FDA product code LOX
Manufacturer City Province Registered as Device types
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Dongguan TT Medical, Inc. Dongguan Guangdong Manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
Shanghai Microport Medical (Group) Co., Ltd. Shanghai Shanghai Specification developer 1
Sino Medical Sciences Technology Inc. Tianjin Tianjin Manufacturer 1

Record

Regulatory record for OTW Takeru
Listed by Kaneka Corporation, Japan
FDA product code LOX
Device type Catheters, Transluminal Coronary Angioplasty, Percutaneous
Device class Class 2
Regulation 21 CFR 870.5100
510(k) K172264
Record published 2018-03-26
Record revised 2019-10-07 (version 3)

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, serial number
Storage Special storage condition: Store in a cool, dry, dark place. Avoid exposure to water, direct sunlight.

Catalogue Numbers

Catalogue numbers for OTW Takeru
Catalogue number Size Status
DC-PY3215UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4520UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3715UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2030UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2706UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2012UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3020UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4515UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY5020UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2720UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1520UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2708UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3720UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3030UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2212UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3012UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2712UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2715UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2208UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2515UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2006UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4020UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2015UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3015UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4008UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3010UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4012UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3212UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2010UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3510UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1515UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4030UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4010UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3508UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2008UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2020UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3220UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2508UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY5008UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4512UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2220UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2512UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2520UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2530UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3520UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3208UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4015UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3512UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1530UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1508UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3008UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1512UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3708UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2215UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3515UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2510UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY4508UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY5015UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2206UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY2506UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1510UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY5012UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3530UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3006UA2 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY1506UA1 Maximum Guidewire Diameter; 0.014 inch In distribution
DC-PY3712UA2 Maximum Guidewire Diameter; 0.014 inch In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
NC Emerge® Boston Scientific Corporation 144
Sprinter® Legend Medtronic, Inc. 133
NC Quantum Apex™ Boston Scientific Corporation 128
Trek Abbott Vascular 120
Emerge™ Boston Scientific Corporation 119
NC Trek Abbott Vascular 118
Apex™ Boston Scientific Corporation 116
Maverick²™ Boston Scientific Corporation 113
Apollo Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 110
Sprinter® Medtronic, Inc. 108
NC Stormer™ OTW Medtronic, Inc. 108
Quantum™ Maverick™ Boston Scientific Corporation 106

Showing 12 of 67. All products under Catheters, Transluminal Coronary Angioplasty, Percutaneous

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K172264 2018-03-19
K170941 2017-07-07
K163372 2017-04-07

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
P020037 2003-06-11 FX MINIRAIL RX PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) CATHETER Abbott Vascular
P790017 2003-03-04 NC STORMER OVER-THE-WIRE BALLOON DILATATION CATHETER AND NC STORMER ZIPPER MX BALLOON DILATATION CATHETER Medtronic Ireland
P880027 2002-06-25 PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) Boston Scientific Corporation
P860019 2000-12-08 MAXXUM AND NC MAXXUM PTCA CATHETER Scimed Life Systems, Inc.
P880003 2000-07-07 NINJA FX PTCA DILATATION CATHETER Cordis Corp.
P990008 1999-09-27 COOK MBC PTCA BALLOON DILATATION CATHETER Cook Incorporated
P960014 1998-10-05 MAGELLAN-C PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY(PTCA) CATHETERS MODEL C22020,C22520,C23020,& C23520 Global Therapeutics, Inc.
P970052 1998-04-08 LYNX CONTOUR CORONARY BALLOON DILATATION CATHETER(A NEW MODEL OF THE FACT CATHETER). Endologix LLC
P930012 1997-05-29 THE WRAP(PTCA) CATHETER Progressive Angioplasty Systems, Inc.
P910031 1996-12-02 FACT(TM)AND ARC BALLOON CORNARY DILATATION CATHETERS Abbott Vascular Devices
P890048 1996-11-26 USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS Usci, Div. C.R. Bard, Inc.
P890001 1996-06-07 LEOCOR PICO RUNNER(TM) PTCA CATHETER Leocor, Inc.
P850021 1995-07-12 HYBRID (PTCA) CATHETER Abbott Vascular
P940009 1994-09-29 PERCUTANEUS TRANSLUMINAL CORONARY ANGIOPLASTY CATH Scimed Life Systems, Inc.
P890032 1992-07-23 CORDIS ORION STEERABLE PTCA BALLOON CATHETER Cordis Corp.
P880055 1991-07-19 MICROSS-SL(TM) PTCA DILATATION CATHETER Boston Scientific Corporation
P840040 1991-01-30 HEART TRAK PTCA CATHETER Boston Scientific Corporation
P810046 1990-10-05 ACS RX(R) –.014 CORONARY DILATATION CATHETER Advanced Cardiovascular Systems, Inc.
P870021 1990-10-04 PRIME{TM} MODEL 6520, 6525, 6530 AND 6535 Medtronic, Inc.
P880065 1990-09-19 MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER Boston Scientific Corporation
P870036 1989-06-23 VERSAFLEX BUCHBINDER OMNIFLEX PTCA CATHETER SYSTEM Medtronics Interventional Vascular

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