Maxim Biomedical Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1122236
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 1122236
- Address
- 1500 E GUDE DR, Rockville, MD, 20850
Frequently asked questions
How many devices does MAXIM BIOMEDICAL INC. have in the registry?
The registry currently lists 2 devices for MAXIM BIOMEDICAL INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MAXIM BIOMEDICAL INC.'s devices?
Among its 2 most recently registered devices, MAXIM BIOMEDICAL INC. has devices listed in FDA GUDID (2 devices).
What risk classes do MAXIM BIOMEDICAL INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for MAXIM BIOMEDICAL INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from MAXIM BIOMEDICAL INC. in the registry?
The most recently registered devices listed for MAXIM BIOMEDICAL INC. include Cambridge Biotech HIV-1 Urine Western Blot 98078 and Maxim HIV-1 Urine EIA 700000.