Sterimed, Inc.
United StatesFDA applicant, unverified FDA FEI 1053306
- Devices
- 465
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sterimed, Inc. makes
Sterimed, Inc. manufactures single-use sterilization packaging, X-ray system covers, medical equipment and instrument drapes, C-arm drapes, camera covers, and sterile and non-sterile cable, lead, sensor, and probe covers. It also produces urological fluid funnels.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) and FDA UDI registries. Sterimed, Inc. is based in the United States.
Catalogue
Search and filter all 465 devicesShowing 1-50 of 465
Company details
- FDA FEI number
- 1053306
- DUNS number
- 182052670
- Address
- 2266 Volvo Car Dr, Ridgeville, SC, 29472
- Phone
- +1(843)388-8080
Frequently asked questions
How many devices does Sterimed, Inc. have in the registry?
The registry currently lists 465 devices for Sterimed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterimed, Inc.'s devices?
Among its 50 most recently registered devices, Sterimed, Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Sterimed, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Sterimed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sterimed, Inc. in the registry?
The most recently registered devices listed for Sterimed, Inc. include Sterimed 4425B, Arjo Wiggins Medical, Inc. 101047AR1515, Arjo Wiggins Medical, Inc. 1011001212D and Sterimed PC0796.