EVO

3 catalogue numbers from Control Unit, listed by LivaNova Deutschland GmbH, Germany, under Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue 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 EVO
Listed by LivaNova Deutschland GmbH, Germany
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) K082344
Record published 2021-05-14
Record revised 2024-05-07 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for EVO
Catalogue number Size Status
Control Unit In distribution
Occluder In distribution
Control Unit 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 EVO
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
LivaNova USA, Inc. 510(k) number 2010-06-18 Not classified PMA Although accessories were designed for use with two models, the HLM C5 and the HLM S5, the submission that included references to the Mast Roller Pump, B-Care5, and the Electrical Venous Line Occluder accessories covered the new HLM S5 syst 1 unit 2010-07-21

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