MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2019-11-07 for 23G MST MICRO-HOLDING FORCEPS DFH-0019 manufactured by Microsurgical Technology.
Report Number | 3019924-2019-00008 |
MDR Report Key | 9291601 |
Report Source | DISTRIBUTOR,FOREIGN |
Date Received | 2019-11-07 |
Date of Report | 2019-11-07 |
Date of Event | 2019-09-26 |
Date Mfgr Received | 2019-10-08 |
Device Manufacturer Date | 2019-01-04 |
Date Added to Maude | 2019-11-07 |
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. CECIL CHRISINGER |
Manufacturer Street | 8415 154TH AVE NE |
Manufacturer City | REDMOND WA 98052 |
Manufacturer Country | US |
Manufacturer Postal | 98052 |
Manufacturer Phone | 4252843754 |
Manufacturer G1 | MICROSURGICAL TECHNOLOGY |
Manufacturer Street | 8415 154TH AVE NE |
Manufacturer City | REDMOND WA 98052 |
Manufacturer Country | US |
Manufacturer Postal Code | 98052 |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 23G MST MICRO-HOLDING FORCEPS |
Generic Name | FORCEPS, OPHTHALMIC |
Product Code | HNR |
Date Received | 2019-11-07 |
Model Number | DFH-0019 |
Catalog Number | DFH-0019 |
Lot Number | 105413 |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICROSURGICAL TECHNOLOGY |
Manufacturer Address | 8415 154TH AVE NE REDMOND WA 98052 US 98052 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-11-07 |