Kodak 2200 Operating Manual
Re: re: re: re: Kodak 2200 Kverror August 12, 2016 09:31 The ceramic resistor is under the tube board. Unsolder the wires connected to internal socket and lift up the tube board carefully. I would recommend you not dismantle the ceramic resistor. Just check if it's ok (13 Kohm and 200 MOhn) and solder unplagged wire to it. The resistor is very fragile! Sometimes the plastic cup bends itself so it pulls up the ceramic resistor.
The voltage devider must be immersed in oil completely, no air bubbles present in oil! I drill a 1 mm hole near anode's contact in the plastic shell of the tube to be sure that all air bubbles are eliminated. Air is a reason of fail in repair. Re: re: re: re: re: re: Kodak 2200 Kverror January 04, 2017 10:23 The soldering on the resistor gets loose and this is the reason why so many of you get error 13.
Once the old solder removed, the wires soldered back with new solder (do not overheat) place the high voltage contact spring and insert the high voltage multiplier block inside the plastic cup containing the feedback resistor. Then insert the assembly gently inside the metal housing, taking care with the position. There are two grooves on the plastic cup that must match those in the bottom of the housing.
If excessive force is applied, then the ceramic resistor will break in pieces! Heating the assembly with hair dryer helps sometimes. Re: re: re: Kodak 2200 Kverror March 06, 2017 08:07 Hi, KV error on a 2200 means either a power board failure or a tubehead failure which is the most frequent problem. Start by measuring the 13 Kohm feedback resistor (located inside the housing) with Ohmmeter between ground and yellow small wire on the tubehead connector once removed from the arm. WARNING: make sure you attach the arm in the closed position before you remove the tubehead. If you find the good value, then check contacts on connecto (arm side), place tube back and check that the resistor reaches the power board by measuring the resistance on the small white connector J6 between black and yellow wire. Send me a mail and I will send you a link to view my technical files or give you more information.
CAS deadlines: action underway 10 March 2014, action complete: 24 March 2014 Note: These deadlines are for systems to be in place to identify affected units and plan any appropriate actions Device Intra-oral dental X-ray units: Kodak 2100 and Kodak 2200 (wall and ceiling mounted) Manufactured by Carestream Health Models released for sale from May 2008 to April 2010, serial numbers as identified in the FSN. Problem Risk of injury if the joint between the scissor arm and bracket fails. This joint could fail prematurely due to a manufacturing problem during the period from May 2008 to April 2010. Action.
Identify affected devices using the guidance in the manufacturer’s (195Kb) (FSN). Inspect the units using the pictures in the FSN, to ensure the arm has not failed. If the unit shows signs of failure, stop using it and call your dealer immediately. All systems need to be inspected even if they don’t show signs of failure.
Kodak Service Manuals
Contact your dealer to arrange a service engineer visit. Action by. Dentists. Community dental practices.
General dental practitioners. Distribution This MDA has been sent to:. Care Quality Commission (CQC) (headquarters) for information. Clinical commissioning groups (CCGs). HSC trusts in Northern Ireland (chief executives).
Local authorities in Scotland (equipment co-ordinators). NHS boards and trusts in Wales (chief executives). NHS boards in Scotland (equipment co-ordinators). NHS England area teams. NHS trusts in England (chief executives) Onward distribution Please bring this notice to the attention of relevant employees in your establishment.
Kodak 2200 Service Manual
Below is a suggested list of recipients. Northern Ireland Adverse Incident Centre Health Estates Investment Group Room 17 Annex 6 Castle Buildings, Stormont Estate Dundonald BT4 3SQ Tel: 02890 523 704 Fax: 02890 523 900 Email: How to report adverse incidents in Northern Ireland Please report directly to NIAIC, further information can be found on the Further information about SABS can be found Scotland All requests regarding return, replacement or modification of the devices mentioned in this alert should be directed to the relevant supplier or manufacturer. Other enquiries and adverse incident reports in Scotland should be addressed to.