21-04-2021

Linn Ekos Serial Numbers



  1. Linn Ekos Serial Numbers Lookup
  2. Linn Ekos Serial Numbers Doreen
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Ekos

Hello All, Texas newbie to this forum and new to owning a Linn product (AV 5150). Hay day farm design images. Ive been searching till I got a headache from all the dead ends (including Linn support). I recently acquired the 5150 and knew it had an issue, however Im retired and somewhat bored so I figured what the heck on th. Linn Ekos 1 Tonearm Serial number 1860 Made Dec 1988 VGC in full working order Included is the Collar/Counterweight/Grey T-Kable/Fixing Bolts No Box/Packing Supplied with 3 months warranty parts and labour. Linn Cartridge Part-Exchange Values Kandid Krystal Kandid 8 00 Akiva 8 00 18 0 Arkiv B 600 18 0 Arkiv 500 18 0 Krystal 300 18 0 Klyde / Troika 200 125 Karma 125 70 Asaka 100 60 B efore any trade -in is agreed, the serial number of the cartridge being tr aded-in mus t be checked with Linn - please contac t orders@linn. Co.uk Turntable Components.

Newsflash: Tidal keeps rejecting my login using Kazoo or Linn App. Click on Product family to expand product range. Klimax Products: Akurate Products: Majik Products. Event reported to ekos: the catheter would not flush properly. The catheter was never placed in a patient. Manufacturer Narrative Although the user facility report indicated the device was a 12 cm ekosonic device, serial number (b)(4), the device returned to ekos for investigation was a 6 cm ekosonic device, serial number (b)(4).

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EKOS CORP. EKOSONIC ENDOVASCULAR SYSTEMBack to Search Results
Model Number 106CM / 12 CM
Device Problems Restricted Flow rate (1248); Improper Flow or Infusion (2954)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 01/27/2015
Event Type Malfunction
Event Description

Event desc: the ekos catheter would not flush properly. The procedure was able to be completed successfully with another ekos catheter. There were no complications. What was the original intended procedure: pulmonary angiogram with hemodynamic pressures. Placement of bilateral 12 cm working length ekos sonothrombolysis catheters. Device usage problem: device failed (e. G. Broke, couldn't get it to work or stopped working). Event reported to ekos: the catheter would not flush properly. The catheter was never placed in a patient.

Manufacturer Narrative

Although the user facility report indicated the device was a 12 cm ekosonic device, serial number (b)(4), the device returned to ekos for investigation was a 6 cm ekosonic device, serial number (b)(4). Additionally, although the customer reported the device was never used in a patient, inspection of the returned device confirmed the drug infusion lumens were filled with dried blood. This condition is consistent with having been placed in a patient and the blood filled infusion lumens also most likely caused the reported event. No patient injury was reported and the patient was reported to have a 'good' outcome.

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Linn Ekos Serial Numbers Lookup


Linn Ekos Serial Numbers Doreen

Manufacturer (Section D)
EKOS CORP.
11911 n creek parkway south
bothell WA 98011
Manufacturer Contact
11911 n creek parkway south
bothell, WA 98011
4254153132
MDR Report Key4861539
MDR Text Key5851076
Report Number3001627457-2015-00004
Device Sequence Number1
Product Code KRA
Combination Product (Y/N)N
Reporter Country CodeUS
PMA/PMN NumberK140151
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source TypeUser facility
Reporter Occupation RISK MANAGER
Type of ReportInitial
Report Date04/23/2015
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received06/18/2015
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device EXPIRATION Date08/01/2017
Device MODEL Number106CM / 12 CM
Device Catalogue Number500-55112
Device LOT Number140827045-001
Was Device Available For Evaluation? Yes
Date Returned to Manufacturer02/17/2015
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA04/01/2015
Distributor Facility Aware Date01/27/2015
Device Age5 mo
Event Location Hospital
Date Manufacturer Received05/15/2015
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured08/27/2014
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial