MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-28 for PKG., ASSY., STRYKEFLOW 2 WITH TIP 0250070520 manufactured by Stryker Endoscopy-san Jose.
Report Number | 0002936485-2019-00265 |
MDR Report Key | 8745429 |
Date Received | 2019-06-28 |
Date of Report | 2019-08-22 |
Date of Event | 2019-05-31 |
Date Mfgr Received | 2019-06-04 |
Device Manufacturer Date | 2019-03-13 |
Date Added to Maude | 2019-06-28 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ANDREA ZENERE |
Manufacturer Street | 5900 OPTICAL COURT |
Manufacturer City | SAN JOSE CA 95138 |
Manufacturer Country | US |
Manufacturer Postal | 95138 |
Manufacturer Phone | 4087542000 |
Manufacturer G1 | STRYKER ENDOSCOPY-SAN JOSE |
Manufacturer Street | 5900 OPTICAL COURT |
Manufacturer City | SAN JOSE CA 95138 |
Manufacturer Country | US |
Manufacturer Postal Code | 95138 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | PKG., ASSY., STRYKEFLOW 2 WITH TIP |
Generic Name | APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED |
Product Code | GCX |
Date Received | 2019-06-28 |
Catalog Number | 0250070520 |
Lot Number | 19072FG2 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER ENDOSCOPY-SAN JOSE |
Manufacturer Address | 5900 OPTICAL COURT SAN JOSE CA 95138 US 95138 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-28 |