MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2005-02-01 for ASAHI AM-BIO SERIES DIALYZER AM-BIO-100 NO.2004.9-1929 manufactured by Asahi Kasei Medical Co., Ltd..
[444552]
Two blood leaks at two patient occurred during hemodialysis treatment. Both blood leaks occurred at the starting of hemodialysis. The both leakages were observed visually, by the leak detector and by the test strip. The blood loss was about 123cc each because the blood inside the dialyzer and tubing was discarded as the extracorporeal circulation set. Both patients were well and no medical treatment was given.
Patient Sequence No: 1, Text Type: D, B5
[6085133]
Two blood leaks at two patient occurred during hemodialysis treatment. Both blood leaks occurred at the starting of hemodialysis. The both leakages were observed visually, by the leak detector and by the test strip. The blood loss was about 123 each because the blood inside the dialyzer and tubing was discarded as the extracorporeal circulation set. Both patients were well and no medical treatment was given.
Patient Sequence No: 2, Text Type: D, B5
| Report Number | 8010002-2006-00002 |
| MDR Report Key | 673090 |
| Report Source | 06 |
| Date Received | 2005-02-01 |
| Date of Report | 2005-02-01 |
| Date Mfgr Received | 2006-01-05 |
| Device Manufacturer Date | 2005-01-01 |
| Date Added to Maude | 2006-02-13 |
| 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 | 0 |
| Manufacturer Contact | SEIICHI LIJIMA, GENERAL MGR |
| Manufacturer Street | 9-1, KANDA MITOSHIROCHO CHIYODA-KU |
| Manufacturer City | TOKYO 101-8482 |
| Manufacturer Country | JA |
| Manufacturer Postal | 101-8482 |
| Manufacturer Phone | 32595892 |
| Manufacturer G1 | ASAHI KASEI MEDICAL OITA PLANT |
| Manufacturer Street | 2111-2 OAZA SATO OITA-PREFECTURE |
| Manufacturer City | OITA-CITY |
| Manufacturer Country | JA |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ASAHI AM-BIO SERIES DIALYZER |
| Generic Name | HEMODIALYZER |
| Product Code | MSE |
| Date Received | 2005-02-01 |
| Model Number | AM-BIO-100 |
| Catalog Number | NO.2004.9-1929 |
| Lot Number | 44XMY3 |
| ID Number | NO RELATION |
| Device Expiration Date | 2007-11-02 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 662398 |
| Manufacturer | ASAHI KASEI MEDICAL CO., LTD. |
| Manufacturer Address | 9-1, KANDA MITOSHIROCHO CHIYODA-KU TOKYO JA 101-8482 |
| Baseline Brand Name | ASAHI AM-BIO SERIES DIALYZERS |
| Baseline Generic Name | HEMODIALYZER |
| Baseline Model No | AM-BIO-100 |
| Baseline Catalog No | NA |
| Baseline ID | NA |
| Baseline Device Family | ASAHI AM-BIO SERIES DIALYZER |
| Baseline Shelf Life Contained | Y |
| Baseline Shelf Life [Months] | 36 |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K983720 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2005-02-01 |
| 2 | 0 | 2005-02-01 |