MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-11-26 for #9 DEAN SCISSORS S9 manufactured by Hu-friedy Mfg. Co. Llc.
Report Number | 1416605-2019-00018 |
MDR Report Key | 9376258 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-11-26 |
Date of Report | 2019-11-26 |
Date of Event | 2019-10-31 |
Date Mfgr Received | 2019-10-31 |
Date Added to Maude | 2019-11-26 |
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 | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS STEPHANIE WASIELEWSKI |
Manufacturer Street | 3232 N ROCKWELL ST |
Manufacturer City | CHICAGO IL 606185935 |
Manufacturer Country | US |
Manufacturer Postal | 606185935 |
Manufacturer Phone | 8472574500 |
Manufacturer G1 | HU-FRIEDY MFG. CO. LLC |
Manufacturer Street | 3232 N ROCKWELL ST |
Manufacturer City | CHICAGO IL 606185935 |
Manufacturer Country | US |
Manufacturer Postal Code | 606185935 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | #9 DEAN SCISSORS |
Generic Name | SCISSORS, SURGICAL TISSUE, DENTAL |
Product Code | EGN |
Date Received | 2019-11-26 |
Model Number | S9 |
Catalog Number | S9 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HU-FRIEDY MFG. CO. LLC |
Manufacturer Address | 3232 N ROCKWELL ST. CHICAGO IL 606185935 US 606185935 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-11-26 |