Sapphire NC 24 Coronary Dilatation Catheter

The Sapphire NC 24 is a rapid-exchange coronary balloon catheter for widening narrowed coronary arteries or bypass grafts. It is also indicated for coronary occlusions in acute myocardial…

Registry build 21.09.26

The Sapphire NC 24 is a rapid-exchange coronary balloon catheter for widening narrowed coronary arteries or bypass grafts. It is also indicated for coronary occlusions in acute myocardial infarction, in-stent restenosis and expansion of balloon-expandable coronary stents after placement.

The catheter advances over a standard-length, 0.014-inch guidewire. The wire enters at the tip and exits through a distal rapid-exchange port. Its minimally compliant balloon is designed for high-pressure dilatation with controlled balloon dimensions.

Balloon Pressure

Rated burst pressure depends on balloon diameter: 24 atmospheres for 1.5 to 3.5 millimetres, 22 atmospheres for 3.75 to 4 millimetres, and 20 atmospheres for 4.5 to 5 millimetres.

12manufacturers in China registered for this device type
98catalogue 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 Sapphire NC 24 Coronary Dilatation Catheter
Listed by OrbusNeich Medical (Shenzhen) Co., Ltd., China
FDA product code LOX
Device type Catheters, Transluminal Coronary Angioplasty, Percutaneous
Device class Class 2
Regulation 21 CFR 870.5100
Establishment Complaint-file establishment, Manufacturer
510(k) K211807
Record published 2022-02-17

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date

Catalogue Numbers

Catalogue numbers for Sapphire NC 24 Coronary Dilatation Catheter
Catalogue number Size Status
493001212 In distribution
491501812 In distribution
494501212 In distribution
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492871012 In distribution
494502212 In distribution
493500812 In distribution
493751512 In distribution
492501212 In distribution
492000812 In distribution
493000812 In distribution
493251012 In distribution
493501212 In distribution
494002612 In distribution
492872612 In distribution
492751512 In distribution
495000812 In distribution
494500812 In distribution
492501512 In distribution
493751212 In distribution
492500812 In distribution
492252612 In distribution
492751012 In distribution
492751212 In distribution
491501012 In distribution
495002612 In distribution
492251212 In distribution
492001812 In distribution
492252212 In distribution
492751812 In distribution
493752612 In distribution
493002212 In distribution
492001212 In distribution
492501012 In distribution
494001512 In distribution
493502612 In distribution
491751212 In distribution
493501512 In distribution
493251212 In distribution
492502212 In distribution
492251512 In distribution
494502612 In distribution
493501812 In distribution
492752212 In distribution
493252212 In distribution
491502212 In distribution
493252612 In distribution
494002212 In distribution
492501812 In distribution
492251012 In distribution
491501512 In distribution
491751012 In distribution
491751812 In distribution
492001512 In distribution
493751012 In distribution
491502612 In distribution
494001212 In distribution
492872212 In distribution
492871812 In distribution
491750812 In distribution
491751512 In distribution
494501512 In distribution
493001512 In distribution
492871512 In distribution
493751812 In distribution
491752612 In distribution
494501012 In distribution
495001212 In distribution
492250812 In distribution
493002612 In distribution
494001812 In distribution
492502612 In distribution
491500812 In distribution
492870812 In distribution
493752212 In distribution
495002212 In distribution
493251812 In distribution
494001012 In distribution
492002212 In distribution
495001012 In distribution
492752612 In distribution
494000812 In distribution
494501812 In distribution
493501012 In distribution
492871212 In distribution
492251812 In distribution
495001812 In distribution
495001512 In distribution
493001012 In distribution
493251512 In distribution
493502212 In distribution
492001012 In distribution
492750812 In distribution
491752212 In distribution
493750812 In distribution
493250812 In distribution
492002612 In distribution
493001812 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
K233499 2024-08-16
K233505 2024-08-15
K211807 2021-10-14

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