Asia Pacific Latex Sdn Bhd
Country not established
- Devices
- 4
What Asia Pacific Latex Sdn Bhd makes
Asia Pacific Latex Sdn Bhd manufactures powder-free patient examination gloves, including nitrile, latex, and latex with polymer coatings. These products are designed for medical and clinical use to reduce allergic reactions and contamination risks during procedures.
The company’s portfolio is classified as Class I medical devices under FDA regulations and is listed in the FDA’s 510(k) registry. The manufacturer is based in the US.
Catalogue
Nitrile Patient Examination Glove Powder Free Ref K982274
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Latex Patient Examination Gloves Ref K924357
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Asia Pacific Latex Sdn Bhd have in the registry?
The registry currently lists 4 devices for Asia Pacific Latex Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Asia Pacific Latex Sdn Bhd's devices?
Among its 4 most recently registered devices, Asia Pacific Latex Sdn Bhd has devices listed in FDA 510(k) (4 devices).
What risk classes do Asia Pacific Latex Sdn Bhd's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Asia Pacific Latex Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Asia Pacific Latex Sdn Bhd in the registry?
The most recently registered devices listed for Asia Pacific Latex Sdn Bhd include NITRILE PATIENT EXAMINATION GLOVE POWDER FREE, ASIA PACIFIC LATEX SDN. BHD. POWDER FREE LATEX EXAMINATION GLOVES, ASIA PACIFIC LATEX SDN. BHD. POLYMER COATED POWDER FREE LATEX EXAMINATION GLOVES and LATEX PATIENT EXAMINATION GLOVES.