FDA Adverse Event
Malfunction
Summary report: N
PROTIME MICROCAUGULATION SYSTEM
MDR report key: 1711739
·
Received September 10, 2009
Report
- Report Number
- 2248721-2009-00421
- Event Type
- Malfunction
- Date Received
- September 10, 2009
- Date of Event
- October 10, 2007
- Report Date
- August 19, 2009
- Manufacturer
- INTERNATIONAL TECHNIDYNE CORP.
- Product Code
- GKP
- PMA / PMN Number
- K951072
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THIS MDR IS SUBMITTED BASED UPON A RETROSPECTIVE REVIEW OF COMPLAINT REPORTS FROM 2007-2008 IN LIGHT OF REVISED ITC MDR EVALUATION PROCEDURES.
Description of Event or Problem · 1
REPORT IS FOR PT 2 OF 2: THE 3.0 INR WITH PROTIME SYS VS 5.4 INR WITH UNSPECIFIED LAB SYS. PT THERAPEUTIC INR RANGE: 2.0 - 3.0. NO REPORT OF ADVERSE EVENT, SERIOUS INJURY, OR INTERVENTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PROTIME MICROCAUGULATION SYSTEM | PROTIME INSTRUMENT | GKP | INTERNATIONAL TECHNIDYNE CORP. | PROTIMEPRO | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 77 YR | Other | COUMADIN |