Vitaltec Corporation
Taiwan Last updated 25 Oct 2026
- Devices
- 10
- Registries
- EUDAMEDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
Venti-Trach Tracheostomy Tube (570 Series) Ref K253063
Rota-Trach Disposable Standard Tracheostomy Tube Ref 5410800
Rota-Trach Inner Cannula Tracheostomy Tube Ref 5510700
Rota-Trach Tracheostomy Tube Model Rota-Trach Ref K100480
Rota-Trach Disposable Standard Tracheostomy Tube Ref 5410700
Rota-Trach Disposable Standard Tracheostomy Tube Ref 5310700
Vital-Cath 72 Closed Suction System Ref 65120
Rota-Trach Disposable Standard Tracheostomy Tube Ref 5310800
Vital-Cath Closed Suction System Ref 60120
Related companies
Authorised representatives
What Vitaltec Corporation makes
Vitaltec Corporation manufactures disposable tracheostomy tubes, including cuffed, fenestrated, and uncuffed variants sized between 6.0–10.0mm, as well as inner cannulas and closed suction systems for tracheostomy care. Products are designed for single-use applications in clinical settings requiring airway management.
The company’s tracheostomy tubes and suction systems are classified as Class II or Class IIa/IIb medical devices, depending on the specific product. These devices are listed in the EU’s eudamed registry and have undergone 510(k) clearance via the FDA’s premarket notification process. The manufacturer is based in Taiwan.
Frequently asked questions
How many devices does Vitaltec Corporation have in the registry?
The registry currently lists 10 devices for Vitaltec Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vitaltec Corporation's devices?
Among its 10 most recently registered devices, Vitaltec Corporation has devices listed in EUDAMED (7 devices) and FDA 510(k) (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Vitaltec Corporation's devices fall under?
Among its 10 most recently registered devices, the classes recorded for Vitaltec Corporation's devices are Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vitaltec Corporation in the registry?
The most recently registered devices listed for Vitaltec Corporation include Venti-Trach Tracheostomy Tube (570 Series), Rota-Trach Disposable Standard Tracheostomy Tube, Rota-Trach Inner Cannula Tracheostomy Tube and ROTA-TRACH TRACHEOSTOMY TUBE MODEL ROTA-TRACH.
Information
- Address
- No.12, Lane 4-30, Chyuan Zhou Rd.,, Hou Li District Taichung
- Website
- vitaltec.com.tw
- [email protected]
- PRRC contact
- Ti-Li Chang
- EUDAMED SRN
- TW-MF-000011422
- FDA FEI number
- 3003851906