M/S Midland Latex Products, Ltd.
Country not established
- Devices
- 1
What M/S Midland Latex Products, Ltd. makes
M/S Midland Latex Products, Ltd. manufactures powder-free, siliconised low-protein latex examination gloves designed for medical and clinical use, reducing the risk of allergic reactions in healthcare professionals and patients.
The company’s product 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 United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does M/S Midland Latex Products, Ltd. have in the registry?
The registry currently lists 1 device for M/S Midland Latex Products, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M/S Midland Latex Products, Ltd.'s devices?
Among its 1 most recently registered device, M/S Midland Latex Products, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do M/S Midland Latex Products, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for M/S Midland Latex Products, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from M/S Midland Latex Products, Ltd. in the registry?
The most recently registered devices listed for M/S Midland Latex Products, Ltd. include LOPRO SILICONISED LOW PROTEIN POWDERFREE LATEX EXAMINATION GLOVES.