Vivo 3

Ventilator, Continuous, Minimal Ventilatory Support, Facility Use

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (3), Fujian (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNT
Manufacturer City Province Registered as Device types
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Respironics Medical Products (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61

Record

Regulatory record for Vivo 3
Listed by Breas Medical, Inc., United States
FDA product code MNT
Device type Sv70 Ventilator
Device class Class 2
Regulation 21 CFR 868.5895
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K240779
Record published 2025-05-19

Specifications

Specifications
MRI safety MR Unsafe
Prescription Prescription only
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Vivo 3
Catalogue number Size Status
Vivo 3 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
BiPAP A40 Respironics Inc. 102
Philips Respironics California, Inc. 29
DreamMapper Respironics Inc. 27
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 25
BiPAP Respironics Inc. 11
EncoreAnywhere Respironics Inc. 10
Care Orchestrator Respironics Inc. 8
A Series Respironics Inc. 7
Nihon Kohden Nihon Kohden Orangemed, LLC 6
Remote Alarm Resmed PTY Ltd. 5
Stellar Resmed PTY Ltd. 5
AF811 Respironics Inc. 4

Showing 12 of 53. All products under Sv70 Ventilator

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K240779 2024-12-13
K090113 2009-05-14
K071702 2008-02-15
K053607 2006-03-16

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