Ansell Perry
Country not established
- Devices
- 22
What Ansell Perry makes
Ansell Perry manufactures powder-free surgical and examination gloves, including polyurethane, latex, and polyvinyl chloride (PVC) varieties. Their products are designed for chemotherapy use, low-protein content claims, and medical examinations, with some featuring polymer coatings or synthetic materials. Examples include latex gloves with protein labeling claims, synthetic surgical gloves for chemotherapy, and examination gloves with reduced water-extractable protein.
The company’s portfolio is classified under Class I medical devices in the U.S. and is listed via FDA 510(k) clearance. Products are regulated under U.S. jurisdiction, with compliance documented through the FDA’s 510(k) pathway. Ansell Perry operates from the United States.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Ansell Perry have in the registry?
The registry currently lists 22 devices for Ansell Perry. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ansell Perry's devices?
Among its 22 most recently registered devices, Ansell Perry has devices listed in FDA 510(k) (22 devices).
What risk classes do Ansell Perry's devices fall under?
Among its 22 most recently registered devices, the classes recorded for Ansell Perry's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ansell Perry in the registry?
The most recently registered devices listed for Ansell Perry include ELITE POWDER-FREE POLYURETHANE SYNTHETIC SURGICAL GLOVES (CHEMOTHERAPY USE), X-TENDA CUFF POWDER FREE LATEX SURGICAL GLOVES WITH PROTEIN CONTENT LABELING CLAIM 50 MICROGRAMS OR LESS, MODEL STYLE 21, DERMA PRENE POWDER-FREE SYNTHETIC SURGICAL GLOVES (CHEMOTHERAPY USE) and DERMACLEAN X-AM (PROTEIN LABELING CLAIM) EXAMINATION GLOVES.