Nasal Jet Tube

30Fr

Registry build 21.09.26
9manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code
1recall

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (2), Zhejiang (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code BTR
Manufacturer City Province Registered as Device types
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Hangzhou Jinlin Medical Appliances Co., Ltd. Hangzhou Zhejiang Contract manufacturer 11
Jiangxi Yikang Medical Instrument Group Co., Ltd. Nanchang Jiangxi Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Jiangsu Weikang Jiejing Medical Apparatus Co., Ltd. Shuyang Jiangsu Contract manufacturer 18
Qingdao Traworks Co., Ltd. Qingdao Shandong Exporter 7
Tianjin Medis Medical Device Co., Ltd. Tianjin Tianjin Contract manufacturer 5
Chilecom Medical Devices Co Ltd Xiangtan Hunan Manufacturer 5

Record

Regulatory record for Nasal Jet Tube
Listed by Well Lead Medical Co., Ltd., China
FDA product code BTR
Device type Tube, Tracheal (W/Wo Connector)
Device class Class 2
Regulation 21 CFR 868.5730
Establishment Contract manufacturer, Contract steriliser, Manufacturer, Exporter
Record published 2022-08-10
Record revised 2025-07-21 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Packaging Box of 10, carton of 10

Catalogue Numbers

Catalogue numbers for Nasal Jet Tube
Catalogue number Size Status
A06A065010 In distribution
A06A067010 In distribution
A06A066010 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Rusch Teleflex Medical LLC 301
Shiley Covidien LP 295
Mallinckrodt Covidien LP 258
Hudson RCI Teleflex Medical LLC 241
Portex ICU Medical, Inc 208
Parker Flex-Tip Salter Labs 164
Parker Salter Labs 157
Curaplex Bound Tree Medical, LLC 149
SourceMark Sourcemark, LLC. 148
Montgomery® Safe-T-Tube™ Boston Medical Products, Inc. 144
Sunmed SunMed Group Holdings, LLC 112
Forsure Forsure Medical Products LLC. 101

Showing 12 of 374. All products under Tube, Tracheal (W/Wo Connector)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211543 2022-07-21
K182739 2019-12-11
K110269 2011-08-26

Recalls

The FDA has not published a severity grade for these. 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
2026-07-31 Not classified Process control The 6Fr suction catheter could not pass through the samples smoothly. 27200

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