Tan Chong Rubber Gloves Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 2
What Tan Chong Rubber Gloves Sdn Bhd makes
Tan Chong Rubber Gloves Sdn Bhd manufactures patient examination gloves, including non-chlorinated powder-free, non-sterile versions and latex-based variants. These products are designed for single-use in clinical settings to reduce direct contact with patients during examinations.
The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Patient Examination Gloves (Latex) Ref K891501
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tan Chong Rubber Gloves Sdn Bhd have in the registry?
The registry currently lists 2 devices for Tan Chong Rubber Gloves Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tan Chong Rubber Gloves Sdn Bhd's devices?
Among its 2 most recently registered devices, Tan Chong Rubber Gloves Sdn Bhd has devices listed in FDA 510(k) (2 devices).
What risk classes do Tan Chong Rubber Gloves Sdn Bhd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tan Chong Rubber Gloves Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tan Chong Rubber Gloves Sdn Bhd in the registry?
The most recently registered devices listed for Tan Chong Rubber Gloves Sdn Bhd include PATIENT EXAMINATION GLOVES (NON-CHLORINATED POWDER FREE, NON-STERILE) and PATIENT EXAMINATION GLOVES (LATEX).