Coronary Artery Perfusion Cannula

Coronary Artery Perfusion Cannula with balloon

Registry build 21.09.26
3manufacturers in China registered for this device type
10catalogue numbers in this listing

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DWF
Manufacturer City Province Registered as Device types
Gcmedica Enterprise Ltd.(Wuxi) Wuxi Jiangsu Contract manufacturer 55
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26

Record

Regulatory record for Coronary Artery Perfusion Cannula
Listed by Vitalcor, Inc., United States
FDA product code DWF
Device type Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device class Class 2
Regulation 21 CFR 870.4210
Establishment Specification developer, Manufacturer
510(k) K030231
Record published 2016-09-16
Record revised 2018-07-06 (version 3)

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
Packaging Case of 5

Catalogue Numbers

Catalogue numbers for Coronary Artery Perfusion Cannula
Catalogue number Size Status
415805 In distribution
315806 In distribution
315808 In distribution
415804 In distribution
315807 In distribution
415807 In distribution
415806 In distribution
315804 In distribution
415808 In distribution
315805 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Medtronic, Inc. 5,237
DLP™ Medtronic, Inc. 804
Bio-Medicus™ Medtronic, Inc. 223
Pemco Inc Pemco, Inc. 137
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass Maquet Cardiopulmonary GmbH 135
Venous cardiopulmonary bypass cannula LivaNova USA, Inc. 97
Eopa™ Medtronic, Inc. 87
Surge Cardiovascular MED Michigan Holdings LLC 80
Arterial cardiopulmonary bypass cannula LivaNova USA, Inc. 79
MC2™ Medtronic, Inc. 66
Select Series® Medtronic, Inc. 63
Edwards Lifesciences Aortic Perfusion Cannula Edwards Lifesciences Technology Sarl 52

Showing 12 of 372. All products under Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Coronary Artery Perfusion Cannula
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
LivaNova USA, Inc. 510(k) number 2016-08-12 Class II Process control The tip of the cannula should be bent at either a 45 or 90 degree angle. Samples have been returned where the angle of the tip is less than the requirement. 1205 units worldwide 2017-03-27

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