Apr 02, 2018 Linn serial numbers wanted please. Linn Sondek LP12 with Ekos arm and Troika cartridge Inception 1972 Manufacturer Linn Products Website The Linn Sondek LP12 (often shortened to Sondek or LP12) is a highly regarded transcription produced by -based, manufacturers of hi-fi, and multi-room audio systems. 'The Ekos came in two generations but the arm wasn't renamed. Ekos II came around 1992, Ekos with serial numbers above 6200 should be IIs. The improvement is changed bearings and the difference is IMO significant. Linn offered rebuilding to the new bearings.' 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). Linn claims that the Keel is an application of its “close-tolerance aluminium machining”, first seen in the ingot casing of the Sondek CD12 CD player. The Keel, along with the Ekos SE tonearm and Trampolin Mk.2 were three Special Edition upgrades for the turntable’s 33⅓ birthday, 33⅓ being the standard rotational speed when playing LPs.
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Linn Ekos Serial Numbers Lookup
| EKOS CORP. EKOSONIC ENDOVASCULAR SYSTEM | Back 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. | | Search Alerts/Recalls |
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Linn Ekos Serial Numbers List
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Linn Ekos Serial Numbers Chart
Linn Ekos Serial Numbers List
Linn Ekos Serial Numbers Lookup
| Manufacturer (Section D) | | EKOS CORP. | | 11911 n creek parkway south | | bothell WA 98011 |
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| Manufacturer Contact | | 11911 n creek parkway south | | bothell, WA 98011 | | 4254153132 |
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| MDR Report Key | 4861539 |
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| MDR Text Key | 5851076 |
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| Report Number | 3001627457-2015-00004 |
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| Device Sequence Number | 1 |
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| Product Code | KRA |
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| Combination Product (Y/N) | N |
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| Reporter Country Code | US |
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| PMA/PMN Number | K140151 |
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| Number of Events Reported | 1 |
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| Summary Report (Y/N) | N |
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| Report Source | Manufacturer |
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| Source Type | User facility |
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| Reporter Occupation | RISK MANAGER |
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| Type of Report | Initial |
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| Report Date | 04/23/2015 |
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| 1 Device Was Involved in the Event |
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| 0 PatientS WERE Involved in the Event: |
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| Date FDA Received | 06/18/2015 |
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| Is This An Adverse Event Report? | No |
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| Is This A Product Problem Report? | Yes |
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| Device Operator | HEALTH PROFESSIONAL |
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| Device EXPIRATION Date | 08/01/2017 |
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| Device MODEL Number | 106CM / 12 CM |
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| Device Catalogue Number | 500-55112 |
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| Device LOT Number | 140827045-001 |
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| Was Device Available For Evaluation? | Yes |
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| Date Returned to Manufacturer | 02/17/2015 |
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| Is The Reporter A Health Professional? | Yes |
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| Was the Report Sent to FDA? | Yes |
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| Date Report Sent to FDA | 04/01/2015 |
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| Distributor Facility Aware Date | 01/27/2015 |
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| Device Age | 5 mo |
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| Event Location | Hospital |
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| Date Manufacturer Received | 05/15/2015 |
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| Was Device Evaluated By Manufacturer? | Yes |
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| Date Device Manufactured | 08/27/2014 |
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| Is The Device Single Use? | Yes |
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| Is this a Reprocessed and Reused Single-Use Device? | No |
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| Type of Device Usage | Initial |
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