5
EN
KAT R Type and T Type Tonometer by KEELER
• Only decontaminate / clean in accordance with a method given in Cleaning (Section 3) of
this instruction manual.
• Use only cloths dampened with water to clean the Applanation Tonometer body. Do not
use corrosive products or alcohol.
• Never use the instrument if the ambient temperature, atmospheric pressure, and / or
relative humidity are outside the limits specified in this manual.
• Should the instrument suffer shocks (for example, should it accidentally fall), follow the
check procedure outlined in the ‘Servicing and Calibrations’ (Section 1); if necessary, return
the instrument to the manufacturer for repair.
• Use only the listed accessories in conjunction with the instrument; use said accessories
only in accordance with the procedures set forth in the instruction manuals.
• Always carefully observe the safety rules and other precautions published herein.
• Do not use in the presence of flammable gases / liquids, or in an oxygen rich environment.
• This device is intended to be used only by suitably trained and authorised healthcare
professionals.
• This product should not be immersed in fluid.
CAUTION
• Use only genuine Keeler approved parts and accessories or device safety and performance
may be compromised.
• Keep out of the reach of children.
• To prevent condensation from forming, allow instrument to come to room temperature
before use.
• For indoor use only (protect from moisture).
• There are no user serviceable parts inside. Contact authorised service representative for
further information.
• Follow guidance on cleaning / routine maintenance to prevent personal injury / damage to
equipment.
• Failure to carry out recommended routine maintenance as per the instructions in this IFU
may reduce the operational lifetime of the product.
• At product end of life dispose of in accordance with local environmental guidelines (WEEE).
2.2 CONTRAINDICATION
There is no restriction to patient population this device can be used with and there are no
known contraindications associated with the device.
• Do not use contact tonometry on those with ruptured globe, corneal lesions, ulcer or
epithelial defects and patients that are not suitable for anesthesia administration.
• Take extra care with patients with ocular infection to prevent transmission.
Summary of Contents for KAT R
Page 1: ...Keeler Applanation Tonometer KAT R type and T type INSTRUCTIONS FOR USE EN HY RU...
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Page 3: ...EN HY RU KAT R T 22 KAT R Type and T Type Tonometer Instructions For Use 1 KAT R 43...
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Page 30: ...26 HY KEELER KAT R T 3 1 Keeler WEEE 2 2...
Page 31: ...27 HY KEELER KAT R T 3 3 1 1 2 70 2 3 4 3 2 1 2 1 1 3 4 10 30...
Page 32: ...28 HY KEELER KAT R T 10 10 30 Pantasept 3 10 3 10 10 10 5 6 60 C 4...
Page 34: ...30 HY KEELER KAT R T 4 60 5 Keeler Fixed R 1 2 3 4 60 5 6 2 0 5 1 2 R T...
Page 35: ...31 HY KEELER KAT R T 60 C 6 3 10X 60 0 5 3 0 Pantasept 3 1...
Page 36: ...32 HY KEELER KAT R T 6 4 10 6 5 1 1 2 1 10 0 3 1...
Page 37: ...33 HY KEELER KAT R T 7 7 1 2...
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Page 42: ...38 HY KEELER KAT R T 10 1 0 0 05 3 0 05 4 10 2 2 5 5 0 2 6 0 2 5 2 1 95 2 05 0 0 3 4 0 2 6 5...
Page 43: ...39 HY KEELER KAT R T 1 95 2 6 2 05 2 7 6 6 5 9 6 1 6 2 2 6 7 6 6 8 9 11 Keeler Keeler Keeler...
Page 46: ...42 HY KEELER KAT R T 15 B2B 01691 676124 44 1691 676124...
Page 51: ...47 KEELER KAT R RU 3 1 Keeler WEEE 2 2...
Page 52: ...48 KEELER KAT R RU 3 3 1 1 2 70 2 3 4 3 2 1 2 1 1 3 4 10 30...
Page 53: ...49 KEELER KAT R RU 10 10 30 Pantasept 3 10 3 10 10 10 5 6 60 4...
Page 55: ...51 KEELER KAT R RU 4 60 5 Keeler R 1 2 3 4 60 5 6 2 0 5 1 2 R...
Page 56: ...52 KEELER KAT R RU 60 6 3 10X 60 Pantasept 0 5 3 0 3 1...
Page 57: ...53 KEELER KAT R RU 6 4 10 6 5 1 1 2 1 10 0 3 1...
Page 58: ...54 KEELER KAT R RU 7 7 1 2...
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Page 63: ...59 KEELER KAT R RU 10 1 0 0 05 3 0 05 4 10 2 2 5 5 0 2 6 0 2 5 2 1 95 2 05 0 0 3 4 0 2 6 5...
Page 64: ...60 KEELER KAT R RU 1 95 2 6 2 05 2 7 6 6 5 9 6 1 6 2 2 6 7 6 6 8 9 11 Keeler Keeler Keeler...
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