MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-06 for COBAS AMPLIPREP INSTRUMENT 03051315001 manufactured by Roche Molecular Systems, Inc..
Report Number | 2243471-2020-00003 |
MDR Report Key | 9678008 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-02-06 |
Date of Report | 2020-02-06 |
Date of Event | 2020-01-16 |
Date Mfgr Received | 2020-01-16 |
Date Added to Maude | 2020-02-06 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | NA STACIE-ANN CREIGHTON |
Manufacturer Street | 1080 US HWY 202 S NA |
Manufacturer City | BRANCHBURG NJ 08876 |
Manufacturer Country | US |
Manufacturer Postal | 08876 |
Manufacturer Phone | 9082537112 |
Manufacturer G1 | ROCHE INTERNATIONAL ROTKREUZ |
Manufacturer Street | FORRENSTRASSE 2 NA |
Manufacturer City | ROTKREUZ 6343 |
Manufacturer Country | CH |
Manufacturer Postal Code | 6343 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COBAS AMPLIPREP INSTRUMENT |
Generic Name | CLINICAL SAMPLE CONCENTRATOR |
Product Code | JJH |
Date Received | 2020-02-06 |
Model Number | NA |
Catalog Number | 03051315001 |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ROCHE MOLECULAR SYSTEMS, INC. |
Manufacturer Address | 1080 US HIGHWAY 202 SOUTH NA BRANCHBURG NJ 08876 US 08876 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-02-06 |