Tabri Gloves Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Tabri Gloves Sdn. Bhd. makes
Tabri Gloves Sdn. Bhd. manufactures latex patient examination gloves designed for clinical use, providing barrier protection during medical procedures and examinations.
The company’s portfolio is regulated under FDA’s Class I device classification and is listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892471
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tabri Gloves Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Tabri Gloves Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tabri Gloves Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Tabri Gloves Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tabri Gloves Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tabri Gloves Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tabri Gloves Sdn. Bhd. in the registry?
The most recently registered devices listed for Tabri Gloves Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).