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Euroimmun US Inc.

Also registered as Euroimmun US, Euroimmun Us, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3007118747

Devices
37
Registrations
FDA
FDA recalls
0

Catalogue37

Newest first, rows 1-37 of 37

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Rows 1-37 of 37

Company details

FDA FEI number
3007118747
Address
1 Bloomfield Ave, Mountain Lakes, NJ, 07046

Frequently asked questions

How many devices does EUROIMMUN US INC. have in the registry?

The registry currently lists 37 devices for EUROIMMUN US INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list EUROIMMUN US INC.'s devices?

Among its 37 most recently registered devices, EUROIMMUN US INC. has devices listed in FDA 510(k) (37 devices).

What risk classes do EUROIMMUN US INC.'s devices fall under?

Among its 37 most recently registered devices, the classes recorded for EUROIMMUN US INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from EUROIMMUN US INC. in the registry?

The most recently registered devices listed for EUROIMMUN US INC. include 25-OH VITAMIN D ELISA, EUROIMMUN IFA Granulocyte Mosaic™ EUROPattern and EUROIMMUN EUROPLUS Granulocyte Mosaic™ EUROPattern, EUROIMMUN ANTI-M2-3E ELISA (IGG) and EUROIMMUN ANTI-GLIADIN (GAF-3X) ELISA (IGA).

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.