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ROCHE SCRIPTS FOR COBAS AMPLICOR CT-NG TEST
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 Contact Information
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| Company Name | ROCHE DIAGNOSTICS CORP. |
| Address | 9115 HAGUE RD. |
| City, State, Zip | INDIANAPOLIS, IN 46250 |
| Country | US |
| FDA Owner/Operator Phone | -- |
| FDA Medical Specialty Code | MI - Microbiology |
| FDA Product Code | LSL |
| FDA Classification Name | DNA-REAGENTS, NEISSERIA |
| FDA Device Classification Code | Standards |
| FDA Regulation Number | 866.3390 |
| FDA Common Generic Name | SEROLOGICAL TEST |
| FDA Proprietary Device Name | ROCHE SCRIPTS FOR COBAS AMPLICOR CT-NG TEST |
| FDA Owner / Operator Number | 1823260 |
| FDA Owner / Operator Name | ROCHE HOLDING, INC. |
| FDA Establishment Registration Number | 1823260 |
| FDA Registered Establishment Name | ROCHE DIAGNOSTICS CORP. |
| FDA Operation Code(s) |
MM - Manufacturer |
| FDA Listing Date | 08-16-06 |
| FDA Listing Status Code | Active |
| Differentiation | N/A |
| Keywords | N/A |
| Description | N/A |
| Brochure | N/A |
| Product Website | N/A |
Competitors of ROCHE DIAGNOSTICS CORP.
Our records indicate that the following medical device companies may manufacture a similar device.
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