VersaTube

VersaTube Tapered Tracheostomy Tube

Registry build 21.09.26
1manufacturer
6catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code BTO
Manufacturer City Province Registered as Device types
Well Lead Medical Co., Ltd. Guangzhou Guangdong Contract manufacturer 46

Record

Regulatory record for VersaTube
Listed by Cook Incorporated, United States
FDA product code BTO
Device type Tube, Tracheostomy (W/Wo Connector)
Device class Class 2
Regulation 21 CFR 868.5800
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2015-10-24
Record revised 2020-08-17 (version 4)

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
Storage Special storage condition: Store in dark, dry, cool place.

Catalogue Numbers

Catalogue numbers for VersaTube
Catalogue number Size Status
G54918 In distribution
G54916 In distribution
G54915 In distribution
G54914 In distribution
G54920 In distribution
G54919 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Tracoe® comfort Tracoe Medical Gmbh 1,296
Portex ICU Medical, Inc 380
Pilling Teleflex Medical LLC 248
Premier Premier Dental Products Co. 111
Tracoe mini Tracoe Medical Gmbh 110
Sklar® Sklar Corporation 70
Laryngotec Andreas Fahl Medizintechnik-Vertrieb GmbH 66
Blom Pulmodyne Inc. 51
Montgomery® Long-Term Cannula Boston Medical Products, Inc. 48
Bivona ICU Medical, Inc 37
Well Lead Tracheostomy Tube Well Lead Medical Co., Ltd. 36
Integra® Jarit® Integra LifeSciences Production Corporation 36

Showing 12 of 77. All products under Tube, Tracheostomy (W/Wo Connector)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K100283 2010-04-23
K870181 1987-05-14

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