MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-24 for FLOWMETER MP01192 manufactured by Dr?gerwerk Ag & Co. Kgaa.
[118393116]
The investigation has just started; results will be provided in a follow-up report.
Patient Sequence No: 1, Text Type: N, H10
[118393117]
It was reported that the pressure dome of a flowmeter came off from the main body when the device was put into operation (pressurized). There was no injury of a person reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9611500-2018-00267 |
MDR Report Key | 7812120 |
Date Received | 2018-08-24 |
Date of Report | 2018-09-28 |
Date of Event | 2018-07-16 |
Date Mfgr Received | 2018-09-25 |
Date Added to Maude | 2018-08-24 |
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 | MS. SONJA HILLMER |
Manufacturer Street | MOISLINGER ALLEE 53-55 |
Manufacturer City | L 23542 |
Manufacturer Country | GM |
Manufacturer Postal | 23542 |
Manufacturer Phone | 4518822868 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | FLOWMETER |
Generic Name | FLOWMETER GAS |
Product Code | CAX |
Date Received | 2018-08-24 |
Model Number | NA |
Catalog Number | MP01192 |
Lot Number | NA |
Device Expiration Date | 2000-01-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DR?GERWERK AG & CO. KGAA |
Manufacturer Address | MOISLINGER ALLEE 53-55 L?BECK 23542 GM 23542 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-08-24 |