Brand Name | LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER |
Type of Device | ENDOSCOPIC MULTIPLE CLIP APPLIER |
Baseline Brand Name | LIGACLIP ENDOSCOPIC MULTIPLE CLIP APPLIER |
Baseline Generic Name | ENDOSCOPIC CLIP APPLIER |
Baseline Catalogue Number | ER320 |
Other Baseline ID Number | BATCH #:J44J8R |
Baseline Device 510(K) Number | |
Baseline Device PMA Number | |
Manufacturer (Section F) |
ETHICON ENDO SURGERY, INC. (CINCINNATI) |
4545 creek rd. |
cincinnati OH 45242 2803 |
|
Manufacturer (Section D) |
ETHICON ENDO SURGERY, INC. (CINCINNATI) |
4545 creek rd. |
cincinnati OH 45242 2803 |
|
Manufacturer (Section G) |
ETHICON ENDO SURGERY, INC. (INDEPENDENCIA) |
blvd independencia #1151 |
|
juarez chihuahua |
MEXICO
|
|
Manufacturer Contact |
gary
leblanc
|
4545 creek rd |
cincinnati
, OH 45242-2803 |
(513)
337
-8582
|
|
Device Event Key | 527535 |
MDR Report Key | 538287 |
Event Key | 511062 |
Report Number | 1527736-2004-00891 |
Device Sequence Number | 1 |
Product Code | GDO |
Report Source |
Manufacturer
|
Source Type |
Company Representative
|
Reporter Occupation |
Other
|
Remedial Action |
Other
|
Type of Report
| Initial |
Report Date |
03/09/2004 |
1 Device Was Involved in the Event | |
1 Patient Was Involved in the Event | |
Date FDA Received | 04/01/2004 |
Is This An Adverse Event Report? |
No
|
Is This A Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Catalogue Number | ER320 |
Device LOT Number | U4YX2Z |
Was Device Available For Evaluation? |
Yes
|
Is The Reporter A Health Professional? |
No
|
Was the Report Sent to FDA? |
No
|
Device Age | unknown |
Event Location |
Not Applicable
|
Date Manufacturer Received | 03/09/2004 |
Was Device Evaluated By Manufacturer? |
No
|
Is The Device Single Use? |
Yes
|
Is this a Reprocessed and Reused Single-Use Device? |
No
|
Is the Device an Implant? |
No
|
Is this an Explanted Device? |
|
Type of Device Usage |
Initial
|