TRAUMEX 1100-01-002 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 1999-07-19 for TRAUMEX 1100-01-002 * manufactured by Fischer Imaging Corp..

Event Text Entries

[126267] The switches on a traumex system stick in the active (in) position.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: 1418957-1999-00005
• MDR Report Key: 233582
• Report Source: 07
• Date Received: 1999-07-19
• Date of Report: 1999-07-19
• Date of Event: 1999-06-17
• Date Mfgr Received: 1999-06-17
• Device Manufacturer Date: 1998-09-01
• Date Added to Maude: 1999-07-30
• 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: 0
• Manufacturer Contact: JANET PRIEUR
• Manufacturer Street: 12300 N. GRANT STREET
• Manufacturer City: DENVER CO 80241
• Manufacturer Country: US
• Manufacturer Postal: 80241
• Manufacturer G1: *
• Manufacturer Street: *
• Manufacturer City: *
• Manufacturer Country: *
• Single Use: 3
• Remedial Action: MA
• Previous Use Code: 3
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: TRAUMEX
• Generic Name: RADIOGRAPHIC SYSTEM
• Product Code: IYB
• Date Received: 1999-07-19
• Model Number: 1100-01-002
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: HEALTH PROFESSIONAL
• Device Availability: N
• Device Eval'ed by Mfgr: N
• Implant Flag: N
• Date Removed: *
• Device Sequence No: 1
• Device Event Key: 226410
• Manufacturer: FISCHER IMAGING CORP.
• Manufacturer Address: 12300 N. GRANT ST. DENVER CO 80241 US
• Baseline Brand Name: TRAUMEX
• Baseline Generic Name: RADIOGRAPHIC SYSTEM
• Baseline Model No: 1100-01-002
• Baseline Catalog No: NA
• Baseline ID: DX TRAUMEX
• Baseline Device Family: TRAUMEX
• Baseline Shelf Life [Months]: NA
• Baseline PMA Flag: N
• Baseline 510K PMN: Y
• Premarket Notification: K880530
• Baseline Preamendment: N
• Baseline Transitional: N
• 510k Exempt: N

Patients

Patient Number	Treatment	Outcome	Date
1	0		1999-07-19