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EUROIMMNUN LEGIONELLA IFA TEST
 Request for Information Form |
 Contact Information
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| Company Name | EUROIMMUN US LLC |
| Address | 429 ROCKAWAY VALLEY RD.
UNIT 1200 |
| City, State, Zip | BOONTON, NJ 07005 |
| Country | US |
| FDA Owner/Operator Phone | 973-402-6101 |
| FDA Medical Specialty Code | MI - Microbiology |
| FDA Product Code | LHL |
| FDA Classification Name | REAGENTS, ANTIBODY, LEGIONELLA, DIRECT & INDIRECT FLUORESCENT |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 866.3300 |
| FDA Common Generic Name | LEGIONELLA IFA TEST |
| FDA Proprietary Device Name | EUROIMMNUN LEGIONELLA IFA TEST |
| FDA Owner / Operator Number | 9066845 |
| FDA Owner / Operator Name | EUROIMMUN US LLC |
| FDA Establishment Registration Number | 3004754465 |
| FDA Registered Establishment Name | EUROIMMUN US LLC |
| FDA Operation Code(s) |
MS - Specification Developer |
| FDA Listing Date | 11-17-06 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of EUROIMMUN US LLC
Our records indicate that the following medical device companies may manufacture a similar device.
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