Case Medical SteriTite Bedienungsanleitung Seite 6

SteriTite® Inspection for Use
The recommended inspection criteria should be performed after each use, because of the variables
associated with cleaning agents and equipment.
1. Perform a visual inspection of all parts prior to each use. Check that gaskets
are properly secured and free of wear or damage. Latches should function
properly. The case and lid should be free of dents that may interfere with the
seal. The aluminum surface of the Container should have no noticeable
corrosion or damage. Be sure filter retention plates or valve plates fit securely.
2. Verify that gaskets in the lid and in the filter retention plate(s) are pliable,
without cracks or tears, and that they are all properly and firmly affixed.
3. Each retention plate should be flat and not warped or dented along the perimeter. The filter should be
present covering each perforated vent. The retention plate should be securely latched when pressing
down at center point. If the retention plate is not properly locked, the filter and retention plate can fall off
onto the contents within the Container compromising the load.
Note: Some rotation of the circular retention plate is a natural occurrence when the filter is in place.
4. Verify that the positioning pin in the lid and base, as well as the label holders on the front of the
SteriTite® container are secure.
5. If the UDI direct mark is no longer readable, the product has reached the end of its useful life and
should be taken out of service.
SteriTite® Assembly for Use
SteriTite® Containers require a disposable filter and filter retention plate as a
microbial barrier. For Containers with a perforated base, place the appropriate
filter over the perforations on the lid and base of the SteriTite® container and
place the filter retention plate over the filter. Secure the filter retention plate
by pushing downwards at center point (where indicated) and rotate the handle
counter-clockwise to close.
Note: Paper filters should be used only for steam and EO sterilization. Non-woven Polypro filters must be
used for H2O2, STERRAD, STERIZONE and V-Pro sterilization, and may be used for pre-vacuum steam and
EO sterilization.
Note: Prepare complex instruments according to the instrument maker's instructions. Use of nonabsorbent
tray liners can cause condensate to pool. Do not use peel pouches within sealed containers, as they cannot
be placed on their side for sterilization.
1. Select the appropriate size basket(s) or tray(s) according to Container size.
2. Arrange the clean instruments in the basket(s) according to hospital procedures. Review the
recommendations provided by the device manufacturer.
Note: MediTray® partitions, brackets and posts are recommended for organization and protection of your
delicate instruments. Place the prepared baskets into the base of the SteriTite® container. Do not exceed
the height of the basket when placing instruments into the basket.
3. To determine container size, add one (1) inch of clearance for proper fit of contents, approximately 1/2
inch from the lid and 1/2 inch from the base. Case Medical has validated its SteriTite® Container system
for stacking multiple layers within the container.
4. Place a process indicator or integrator in opposing corners of the
instrument basket.
Note: Place the indicator in the area of the Container considered to be least
accessible to sterilant penetration. The corners of the Container and the
underside of the lid, away from the filters, are the most likely locations for
air pockets.
Copyright 2020 Case Medical, Inc.®
6
IFU-CASETRANS Rev. 004A
E
n
g
l
i
s
h