Ventilator, Non-Continuous (Respirator)

The FaceFit Ported NIV Mask directs airflow from a CPAP or bilevel positive-airway-pressure device to an adult patient’s nose and mouth. This medium-size mask is intended for hospital…

Registry build 21.09.26

The FaceFit Ported NIV Mask directs airflow from a CPAP or bilevel positive-airway-pressure device to an adult patient’s nose and mouth. This medium-size mask is intended for hospital treatment of one patient for up to 24 hours, after which it is discarded.

An adjustable harness holds the mask’s seal against the face. Vent holes allow exhaled carbon dioxide to leave the mask, and an anti-asphyxiation valve allows spontaneous breathing if the machine fails or the system disconnects.

Listed Item

Facefit NIV Mask With Port Medium

Connections

The mask uses a 22-millimetre male connection for the breathing hose. Auxiliary ports permit oxygen supply or pressure monitoring, and a quick-release strap clip allows the mask to be removed.

18manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (8), Jiangsu (2), Zhejiang (2). 9 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BZD
Manufacturer City Province Registered as Device types
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Modern Medical Equipment Manufacturing Ltd. Heng Li, Dongguan Guangdong Contract manufacturer 26
Suzhou Avon Textile Co., Ltd. Suzhou Jiangsu Contract manufacturer 12
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Respironics Medical Products (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Hunan Beyond Medical Technology Co., Ltd. Changsha Hunan Contract manufacturer 3
Shanghai Baron Technologies Co Ltd Shanghai Shanghai Contract manufacturer 3
BMC(Dongguan) Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Zhejiang Baron Technologies Co., Ltd. Pinghu Zhejiang Contract manufacturer 1
Modern Medical Equipment Manufacturing (Qing Yuan) Ltd Qing Yuan Guangdong Contract manufacturer 26
Shenzhen Sany Pioneer Technology Co., Ltd. Shenzhen Guangdong Manufacturer 9
Resvent Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 6

Showing 12 of 18. All 18 manufacturers in China registered for Ventilator, Non-Continuous (Respirator)

Record

Regulatory record for Ventilator, Non-Continuous (Respirator)
Listed by Intersurgical Ltd., United Kingdom
FDA product code BZD
Device type Ventilator, Non-Continuous (Respirator)
Device class Class 2
Regulation 21 CFR 868.5905
Establishment Specification developer, Complaint-file establishment, Manufacturer, Exporter
510(k) K121747
Record published 2016-09-24
Record revised 2025-02-11 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, manufacturing date
Packaging Pack of 12
Distribution end date 2018-02-13
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Ventilator, Non-Continuous (Respirator)
Catalogue number Size Status
2252030 Withdrawn
2250030 Withdrawn
2251030 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DreamStation Respironics Inc. 386
DreamWear Respironics Inc. 183
REMstar System One 60 Series Respironics Inc. 163
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 152
DeVilbiss DeVilbiss Healthcare LLC. 136
Ventilator, Non-Continuous (Respirator) Hans Rudolph, Inc. 115
BiPAP System One 60 Series Respironics Inc. 105
Ventilator, Non-Continuous (Respirator) Salter Labs 85
BiTrac Select Pulmodyne Inc. 79
Yuwell Sleep Apnea Breathing Therapy Mask Suzhou Yuyue Medical Technology Co., Ltd. 76
AF541 Respironics Inc. 71
CPAP Masks Sunset Healthcare Solutions, Inc. 69

Showing 12 of 699. All products under Ventilator, Non-Continuous (Respirator)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121747 2013-03-14

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