MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 02,06 report with the FDA on 1997-01-03 for TROPHOCAN CVS CATHETER 4870-26 manufactured by Smiths Industries Medical Systems, Inc..
[81255]
During the cvs procedure, a left ovarian corpus luteal cyst was seen measuring 3. 1 x 3. 3 x 2. 4 cma. No adnexal masses or free fluid were visualized. The amniotic fluid volume appeared normal.
Patient Sequence No: 1, Text Type: D, B5
[7830570]
A. 4, d. 6. Unk - follow-up with the hospital reveals that this info is unk because it was not recorded on the patient's chart. Note: no additional info is available for section f because this event was not reported by the initial reporter to the user facilities mdr contact person.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1217052-1997-00001 |
MDR Report Key | 63261 |
Report Source | 02,06 |
Date Received | 1997-01-03 |
Date of Report | 1996-12-02 |
Date of Event | 1996-05-28 |
Date Mfgr Received | 1996-12-02 |
Date Added to Maude | 1997-01-22 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TROPHOCAN CVS CATHETER |
Generic Name | CATHETER, SAMPLING, CHORIONIC VILLUS |
Product Code | LLX |
Date Received | 1997-01-03 |
Model Number | NA |
Catalog Number | 4870-26 |
Lot Number | UNK |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | NO INFO |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 63442 |
Manufacturer | SMITHS INDUSTRIES MEDICAL SYSTEMS, INC. |
Manufacturer Address | 15 KIT ST. KEENE NH 03431 US |
Baseline Brand Name | TROPHOCAN CVS CATHETER |
Baseline Generic Name | CATHETER, SAMPLING, CHORIONIC VILLUS |
Baseline Model No | NA |
Baseline Catalog No | 4870-26 |
Baseline ID | NA |
Baseline Device Family | NA |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 60 |
Baseline PMA Flag | Y |
Premarket Approval | P8900 |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 1997-01-03 |