VivaSight™ 2 DLT Kit 39 Fr – Left

VivaSight 2 DLT Kit 39 Fr - LEFT

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Henan (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code CBI
Manufacturer City Province Registered as Device types
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46
Shenzhen Insighters Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Henan Tuoren Medical Device Co., Ltd. Changyuan Henan Manufacturer 5
Hangzhou Tappa Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 3

Record

Regulatory record for VivaSight™ 2 DLT Kit 39 Fr – Left
Listed by Ambu A/S, Denmark
FDA product code CBI
Device type Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)
Device class Class 2
Regulation 21 CFR 868.5740
Establishment Specification developer, Private-label distributor, Manufacturer, Exporter
Record published 2021-06-25
Record revised 2026-01-30 (version 2)

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, expiry date
Storage Storage environment temperature 10 to 25 °C; Handling environment humidity 30 to 75 % RH; Handling environment temperature 10 to 35 °C
Packaging Pack of 5
Sizes Lumen/inner diameter 4.8 mm; outer diameter 11.5 mm

Catalogue Numbers

Catalogue numbers for VivaSight™ 2 DLT Kit 39 Fr – Left
Catalogue number Size Status
412391000 Lumen/Inner Diameter 4.8 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Insighters Shenzhen Insighters Medical Technology Co., Ltd. 39
Rusch Teleflex Medical LLC 26
Univent Tube (TCB Type) Fuji Systems Corp. 22
Hudson RCI Teleflex Medical LLC 21
Sheridan Teleflex Medical LLC 19
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) Henan Tuoren Medical Device Co., Ltd. 18
Parker Flex-Tip Salter Labs 18
Parker Salter Labs 17
Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) Hangzhou Tappa Medical Technology Co., Ltd. 12
Forsure Forsure Medical Products LLC. 12
Endobronchial Tube Well Lead Medical Co., Ltd. 12
Portex ICU Medical, Inc 11

Showing 12 of 29. All products under Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K203749 2021-05-03

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