Aerogen® Professional Nebulizer System

T-Piece, Ped/ Neo (Polysulphone) (Annealed) (P/N 10-057) and Plug (P/N 10-040) Assembly

Registry build 21.09.26
42manufacturers in China registered for this device type
26catalogue numbers in this listing
9510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Guangdong (23), Jiangsu (7), Fujian (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CAF
Manufacturer City Province Registered as Device types
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
Polymed (Xiamen) Plastic Industrial Co., Ltd. Xiamen Fujian Contract manufacturer 17
Sunmed AP, Ltd., Warehouse NO. 2 Zhuhai Guangdong Contract manufacturer 16
Hangzhou Jinlin Medical Appliances Co., Ltd. Hangzhou Zhejiang Contract manufacturer 11
Shenzhen Huayan E-Commerce Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Shenzhen BI-Rich Medical Devices Co., Ltd. Shenzhen Guangdong Contract manufacturer 9
Respironics Medical Products (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Omron (Dalian) Co., Ltd. (Plant 1) Dalian Liaoning Contract manufacturer 7
Apex Medical (Kunshan) Corp. Kunshan Jiangsu Contract manufacturer 4
Dongguan Polygreen Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Living Science Co., Ltd. Suzhou Jiangsu Contract manufacturer 3

Showing 12 of 42. All 42 manufacturers in China registered for Nebulizer (Direct Patient Interface)

Record

Regulatory record for Aerogen® Professional Nebulizer System
Listed by Aerogen Ltd, Ireland
FDA product code CAF
Device type Nebulizer (Direct Patient Interface)
Device class Class 2
Regulation 21 CFR 868.5630
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K021175
Record published 2016-09-16
Record revised 2025-09-24 (version 7)

Specifications

Specifications
MRI safety MR Unsafe
Prescription Prescription only
Label carries lot or batch number
Storage Storage environment humidity 15 to 95 % RH; Storage environment atmospheric pressure 450 to 1100 millibar; Storage environment atmospheric pressure -20 to 60 °C
Distribution end date 2018-09-24

Catalogue Numbers

Catalogue numbers for Aerogen® Professional Nebulizer System
Catalogue number Size Status
60-043 In distribution
60-044 In distribution
60-042 In distribution
AG-AP1036 Withdrawn
AG-AP1010 Withdrawn
10-061 Withdrawn
AG-AP1200 Withdrawn
AG-AP1015 Withdrawn
AG-AP1100 Withdrawn
AG-AP6000-US Withdrawn
AG-AP1500-US Withdrawn
10-068 Withdrawn
AG-AP1000 Withdrawn
AG-AP1035 Withdrawn
10-056 Withdrawn
AG-AP1020 Withdrawn
90-002 Withdrawn
10-058 Withdrawn
AG-AP1055 Withdrawn
90-007 Withdrawn
10-060 Withdrawn
AG-AP1025 Withdrawn
AG-AP1065 Withdrawn
AG-AP1050-US Withdrawn
10-059 Withdrawn
60-032 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hudson RCI Teleflex Medical LLC 220
AirLife Carefusion 77
AirLife™ Airlife, Inc. 76
Ventlab Ventlab, LLC 56
I-neb Respironics Respiratory Drug Delivery (Uk), Ltd. 55
Aerogen® Solo Nebulizer System Aerogen Ltd 53
Portex ICU Medical, Inc 50
Sidestream Respironics Respiratory Drug Delivery (Uk), Ltd. 48
Hudson RCI Medline Industries, Inc. 46
DeVilbiss DeVilbiss Healthcare LLC. 45
Drive Drive DeVilbiss Healthcare 42
Drivemedical Drive DeVilbiss Healthcare 40

Showing 12 of 541. All products under Nebulizer (Direct Patient Interface)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K232507 2024-05-10
K143719 2015-07-10
K133360 2014-10-17
K120939 2012-04-26
K103635 2011-05-13
K032849 2003-11-21
K021175 2002-05-15
K003022 2000-10-13
K992831 2000-08-25

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Aerogen® Professional Nebulizer System
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Aerogen Ltd 510(k) number 2014-09-02 Class II Nonconforming Material/Component Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had b 2,421 power adapters 2016-04-25
Aerogen Ltd 510(k) number 2014-09-02 Class II Nonconforming Material/Component Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had b 1,223 power adapters 2016-04-25
Aerogen Ltd 510(k) number 2014-09-02 Class II Nonconforming Material/Component Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had b 36 power adapters 2016-04-25
Aerogen Ltd 510(k) number 2014-09-02 Class II Nonconforming Material/Component Aerogen has received a small number of complaints in relation to the main power adapter manufactured by FRIWO GmbH and used in the Aeroneb Solo and Pro Nebuliser systems. The complaints received identified that the power adapter cover had b 323 power adapters 2016-04-25

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