MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-19 for PENTAX FI-16RBS manufactured by Hoya Corporation Pentax Tokyo Office.
Report Number | 9610877-2019-00224 |
MDR Report Key | 8712000 |
Date Received | 2019-06-19 |
Date of Report | 2019-02-01 |
Date of Event | 2019-02-01 |
Date Facility Aware | 2019-02-01 |
Report Date | 2019-06-19 |
Date Reported to FDA | 2019-06-19 |
Date Reported to Mfgr | 2019-06-19 |
Date Mfgr Received | 2019-02-01 |
Device Manufacturer Date | 2004-03-22 |
Date Added to Maude | 2019-06-19 |
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 | MR. WILLIAM GOELLER (TEMPORARY) |
Manufacturer Street | 3 PARAGON DRIVE |
Manufacturer City | MONTVALE NJ 07645 |
Manufacturer Country | US |
Manufacturer Postal | 07645 |
Manufacturer Phone | 8004315880 |
Manufacturer G1 | HOYA CORPORATION PENTAX TOKYO OFFICE |
Manufacturer Street | TSUTSUJIGAOKA 1-1-110 AKISHIMA-SHI |
Manufacturer City | TOKYO, 196-0012 |
Manufacturer Country | JA |
Manufacturer Postal Code | 196-0012 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | PENTAX |
Generic Name | FIBER INTUBATION SCOPE |
Product Code | CAL |
Date Received | 2019-06-19 |
Model Number | FI-16RBS |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 15 YR |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HOYA CORPORATION PENTAX TOKYO OFFICE |
Manufacturer Address | TSUTSUJIGAOKA 1-1-110 AKISHIMA-SHI TOKYO, 196-0012 JA 196-0012 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-19 |