Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040279832

FEI Number

3040279832

Entity Name

VITALTEC CORPORATION

City/State/Country

Taichung, TW

Establishment Address

No. 12, Lane 4-30, Chyuan-Zhou Rd., Hou-Li Dist.,, Taichung 42142, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Vitaltec Corporation (Owner Number: 10091432)

Owner / Operator Contact Address

No. 12, Lane 4-30, Chyuan-Zhou Rd., Hou-Li Dist.,, Taichung, TW-NOTA 42142, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K242921

PMA Number

N/A

All Registered Proprietary Names

Rota-Trach Disposable Standard Tracheostomy Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTO	Tube, Tracheostomy (W/Wo Connector)	Anesthesiology	Class 2	868.5800	2025-07-22

Official Correspondent

Ti-Li Chang

US Agent Details

Travis Hsu Business: Qualtech Consulting LLC Email: travis@qualtechs.com Phone: (626) 3455899

Related Public Records

Same Entity

Vitaltec Corporation

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040279832. Last updated year: 2026. Please use registration number 3040279832 when referencing this establishment in official correspondence.