HA01

Respiratory Gas Humidifier

Registry build 21.09.26
12manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (7), Jiangsu (2), Fujian (1). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BTT
Manufacturer City Province Registered as Device types
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Shenzhen MED-Link Electronics Tech Co., Ltd. Shenzhen Guangdong Contract manufacturer 18
Jianerkang Medical Co., Ltd. Changzhou Jiangsu Contract manufacturer 18
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
Sunmed AP, Ltd., Warehouse NO. 2 Zhuhai Guangdong Contract manufacturer 16
Beijing Aeonmed Co., Ltd. Sanhe Hebei Contract manufacturer 7
Betacera Inc. Suzhou Jiangsu Contract manufacturer 3
Chinamed Products (China) Ltd. Gaoyao District Guangdong Manufacturer 8
Ninghai Guangjie Electronic Commerce Co., Ltd. Ningbo Zhejiang Manufacturer 3
Vincent Medical(Dongguan)Technology Company Limited Dongguan Guangdong Contract manufacturer 2

Record

Regulatory record for HA01
Listed by Breas Medical, Inc., United States
FDA product code BTT
Device type Humidifier, Respiratory Gas, (Direct Patient Interface)
Device class Class 2
Regulation 21 CFR 868.5450
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-20
Record revised 2022-06-17 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Packaging Box
Distribution end date 2021-12-16

Catalogue Numbers

Catalogue numbers for HA01
Catalogue number Size Status
US Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hudson RCI Teleflex Medical LLC 160
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 151
Vapotherm Vapotherm Inc. 134
Humidifier, Respiratory Gas, (Direct Patient Interface) Salter Labs 96
Hudson RCI Medline Industries, Inc. 41
AirLife™ Airlife, Inc. 27
Fisher and Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 20
F&P Optiflow Junior 2 Fisher & Paykel Healthcare, Ltd. 17
MR850 Fisher & Paykel Healthcare, Ltd. 13
AirLife Carefusion 13
softFlow TNI Medical AG 11
F&P Optiflow+ Fisher & Paykel Healthcare, Ltd. 7

Showing 12 of 138. All products under Humidifier, Respiratory Gas, (Direct Patient Interface)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K060790 2006-05-25

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