Hudson RCI

HUMID-VENT 2S with SOFT FLEX Tube, Assembled

Registry build 21.09.26
29manufacturers in China registered for this device type
34catalogue numbers in this listing
5recalls on this code

Who Else Makes It

Concentrated in Zhejiang (10), Guangdong (8), Jiangsu (5). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BYD
Manufacturer City Province Registered as Device types
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Amsino Medical (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 22
Zhejiang Haisheng Medical Device Co., Ltd. Shaoxing Zhejiang Contract manufacturer 21
Sunmed AP, Ltd. Zhuhai Guangdong Contract manufacturer 18
Sunmed AP, Ltd., Warehouse NO. 2 Zhuhai Guangdong Contract manufacturer 16
IPE Plastic & Hardware Industy, Ltd Dongguan Guangdong Contract manufacturer 15
VR Medical Technology Co., Ltd. Kunshan Jiangsu Contract manufacturer 13
Zhejiang Runqiang Medical Instruments Co., Ltd. Jiaxing Zhejiang Contract manufacturer 9
Ningbo Boya Medical Equipment Co., Ltd. Yuyao Zhejiang Contract manufacturer 8
GVS Technology (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 5
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263

Showing 12 of 29. All 29 manufacturers in China registered for Condenser, Heat And Moisture (Artificial Nose)

Record

Regulatory record for Hudson RCI
Listed by Teleflex Medical LLC, United States
FDA product code BYD
Device type Condenser, Heat And Moisture (Artificial Nose)
Device class Class 1
Regulation 21 CFR 868.5375
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K945359
Record published 2018-09-15
Record revised 2025-02-07 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Case of 10, case of 30, box of 50, case of 20, box of 25, box of 20
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Hudson RCI
Catalogue number Size Status
IPN040673 In distribution
IPN042602 In distribution
IPN042623 In distribution
IPN916669 In distribution
IPN041384 In distribution
IPN042636 In distribution
IPN913719 In distribution
IPN042634 In distribution
IPN916670 In distribution
IPN043826 In distribution
IPN047605 In distribution
IPN045032 In distribution
IPN042605 In distribution
IPN044420 In distribution
IPN042780 In distribution
IPN044529 In distribution
IPN044418 In distribution
IPN916672 In distribution
IPN916671 In distribution
IPN042781 In distribution
IPN042600 In distribution
IPN042629 In distribution
IPN047604 In distribution
IPN044392 In distribution
IPN041386 In distribution
IPN042597 In distribution
IPN042626 In distribution
IPN913681 In distribution
IPN042477 In distribution
IPN042609 In distribution
IPN042596 In distribution
IPN042619 In distribution
IPN044386 In distribution
IPN044403 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Portex ICU Medical, Inc 34
Gibeck Teleflex Medical LLC 27
iCOR Teleflex Medical LLC 23
DAR Covidien LP 21
AirLife™ Airlife, Inc. 20
Medisize® Medisize B.V. 19
AirLife™ Vyaire Medical, Inc. 13
HME Pepper Medical, Inc. 11
ThermoFlo® Typenex Medical, LLC 11
InHealth Technologies; Blom-Singer Freudenberg Medical, LLC 11
Heat Moisture Exchanger Sunset Healthcare Solutions, Inc. 9
Closed Suction System VR Medical Technology Co., Ltd. 7

Showing 12 of 219. All products under Condenser, Heat And Moisture (Artificial Nose)

Recalls

2 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2022-04-11 Class II Device Design Reports received of torn corrugated breathing tubes. 59,581 eaches
2015-12-03 Class II Device Design Cracking may occur at the 15mm and 22mm ISO female
connector.
2,700 units 2017-01-24
2015-12-03 Class II Release of Material/Component prior to receiving test results Cracks may occur at the 15mm and 22mm ISO female connector. 2,700 ea. 2017-04-14
2015-01-12 Class I Process control Defects: Cracks that may occur in the center of the corrugated flex tube of the 15 mm and 22 mm ISO female connector. 100 units 2016-05-10
2014-12-04 Class I Process control Connector mount cracks which may lead to a leak failure during use and necessitate immediate replacement in the breathing circuit. If leak exists and is left untreated, patient may be deprived of adequate anesthetic gases over a period of 18 2017-03-21

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