Taiwan Link Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 2
What Taiwan Link Sdn Bhd makes
Taiwan Link Sdn Bhd manufactures latex patient examination gloves designed for medical and clinical use, providing barrier protection during procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891505
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K891801
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Taiwan Link Sdn Bhd have in the registry?
The registry currently lists 2 devices for Taiwan Link Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Taiwan Link Sdn Bhd's devices?
Among its 2 most recently registered devices, Taiwan Link Sdn Bhd has devices listed in FDA 510(k) (2 devices).
What risk classes do Taiwan Link Sdn Bhd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Taiwan Link Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Taiwan Link Sdn Bhd in the registry?
The most recently registered devices listed for Taiwan Link Sdn Bhd include PATIENT EXAMINATION GLOVES (LATEX).