TubeChek-B

Ambu TubeChek B, Bulb model Minimum order sales is 20 pcs.

Registry build 21.09.26
9manufacturers in China registered for this device type
2catalogue numbers in this listing
2510(k) clearances naming this product code

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 TubeChek-B
Listed by Ambu A/S, Denmark
FDA product code BTR
Device type Tube, Tracheal (W/Wo Connector)
Device class Class 2
Regulation 21 CFR 868.5730
Establishment Specification developer, Private-label distributor, Manufacturer, Exporter
Record published 2016-01-07
Record revised 2026-01-30 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Storage Storage environment temperature -40 to 60 °C; Handling environment temperature up to 50 °C
Packaging Pack of 8, pack of 20
Sizes Weight 45 g; outer diameter 59 mm; length 83 mm
Distribution end date 2022-02-10

Catalogue Numbers

Catalogue numbers for TubeChek-B
Catalogue number Size Status
000172002 Withdrawn
000172002 Weight 45 g Withdrawn

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
K110962 2011-11-18
K093186 2010-04-16

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