Sakura Seiki Tissue-Tek Glas g2 Скачать руководство пользователя страница 11

AI0-IF-025-00 

9/9 

Certificate of Decontamination (Sample) 

 

 

End of document. 

If you are returning any used medical device to Sakura Finetek Group, please provide the following information 
to help prevent contamination of other devices, etc., or living environment at our facility and the workers who 
will be working on/handling your device. Fill out this Certificate of Decontamination and return it with the device. 
If the device is not accompanied by this certificate, we will not unpack or repair the instrument. If the returned 
medical device is deemed hazardous by Sakura Finetek Group, we will return the device to you immediately. 
The cost of shipment will be borne by you. 

 

 

  Date: 

 

  Institution name: 

 

 

  Equipment information

 

 

[Instrument name]   

[Model]   

[Serial number]   

 

 

 
 

  Please answer the following questions regarding the usage status. (Circle where applicable. Use the Remarks field, if 

necessary.) 

 

 

 

Question 

 

Answer

 

Remarks

 

1. Has this device been used at a hospital where legally designated 

communicable diseases are treated? 

 

Yes

 

No

   

2.  Has  this  device  been  used  in  a  ward  where  patients  of  legally 

designated communicable diseases are staying? 

 

Yes

 

No

   

3. Has this device been used in a room where pathological work on 

infectious diseases is conducted? 

 

Yes

 

No

   

4. Has this device been used in a room where testing of infectious 

diseases is conducted? 

 

Yes

 

No

   

5.  Has  this  device  been  used  in  a  room  where  articles  used  in 

connection with infectious diseases are disposed of? 

 

Yes

 

No

   

6. Has this device been used in a room where research on special 

viruses is conducted? 

 

Yes

 

No

   

7.  Has  this  device  been  used  in  a  room  where  articles  used  in 

connection with special viruses are disposed of? 

 

Yes

 

No

   

 

 

 

 

 

 

  Please answer questions regarding disinfection. 

 

Whenever possible, please return the device after cleaning/disinfecting it using general disinfectant, primarily in areas 
that likely came in contact with tissues, operators, etc. 

 

Examples  of  general  disinfectants:  Disinfecting  alcohol,  70%  isopropanol,  biguanide  alcohol,  benzalkonium  chloride, 
Chlorhexidine

 

 
 

1. Date of disinfection   

 

 

 

 

2. Method of disinfection   

 

 

 

 

 

 

  Remarks 

 

 

 

Содержание Tissue-Tek Glas g2

Страница 1: ...mated Glass Coverslipper This document is a supplement to the following applicable operating manual in order to comply with IVDR requirements Document code 0002783 01 Rev D Manufacturer Sakura Seiki Co Ltd 75 5 Imojiya Chikuma city Nagano 387 0015 Japan www sakurajp com Tel 81 26 272 2381 ...

Страница 2: ...Document code AI0 IF 025 00 Revision history Version Date of revision Revision details 00 Mar 15 2022 First version ...

Страница 3: ...ange the description of BIOHAZARD symbol Be sure to wear protective gears gloves masks goggles etc to prevent infection when using inspecting or disassembling the instrument labeled with this symbol Also wash your hands thoroughly after finishing the work P 1 7 Specifications Add Major components and expected life section Product life 8 years after shipment from manufacturer When replacing consuma...

Страница 4: ...SA C22 2 No 61010 1 UL 61010 2 101 CSA C22 2 No 61010 2 101 For Model 6501 Amendment of Pharmaceutical Affairs Law JIS C 1010 1 JIS C 1010 2 101 JIS C1806 2 6 JIS T 14971 ISO 13485 IEC 62366 IEC 62304 For Model 6502 CE Marking Regulation EU 2017 746 EN 61010 1 EN 61010 2 101 EN 61326 2 6 EN 62366 IEC 62304 EN ISO 18113 1 EN ISO 18113 3 EN ISO 14971 Directive 2011 65 EU EU 2015 863 P 2 1 Installati...

Страница 5: ... soak the instrument in a commercial chemical cleaner for staining solution or bleach cleaner both concentrations are as specified by the commercial product and then wash it with a neutral detergent Also stains may not be completely removed even after cleaning Change the statement of Carbon filter replacement frequency to the following Activated carbon filter Replace the carbon filter with a new o...

Страница 6: ...c by calling toll free 1 800 725 8723 8723 Menu Option 2 If located within the EU contact the following Contact us Products and Security Information Sakura Finetek Europe B V Flemingweg 10a 2408 AV Alphen aan den Rijn NL URL https www sakura eu e mail support sakura eu phone 31 0 88 592 00 90 In countries other than the above contact the nearest authorized Sakura instrument distributor or represen...

Страница 7: ...ing the cover When opening closing a cover or a door be careful not to pinch your body a hand etc between the fixed and moving parts of a cover or between a cover and a door etc Your hand may be pinched and injured P B 2 Cautions Add Check that the facility has a ventilation system a local exhaust system or an exhaust port to the outdoors The amount of volatile gas emitted from the instrument chan...

Страница 8: ...cause injury Add a caution on preventing injuries from slide glass When the slide glass or the cover glass is broken or falls into the instrument remove all glass fragments while being careful not to cut yourself P C 2 Notes on use Add a caution for connecting with Tissue Tek Prisma Plus When connecting the instrument with Tissue Tek Prisma Plus confirm that the lid is not set on the loading stati...

Страница 9: ...risks Flammable reagents solvents and cleaning agents The product uses a Laser beam UK conformity assessed General mandatory action sign General prohibition sign Alternating current Power ON Power OFF P the forth page of the cover P ⅲ TABLE OF CONTENTS P 1 1 General Description P 2 7 Link System P 4 17 How to Operate the Replace Tissue Tek Prisma with the following Tissue Tek Prisma Plus ...

Страница 10: ...AI0 IF 025 00 8 9 Tissue Tek Glas g2 when Linked to the Tissue Tek Prisma Slide Stainer P 4 18 4 19 How to start the Prisma Appendix Add a Certificate of Decontamination sample on the next page ...

Страница 11: ...t a hospital where legally designated communicable diseases are treated Yes No 2 Has this device been used in a ward where patients of legally designated communicable diseases are staying Yes No 3 Has this device been used in a room where pathological work on infectious diseases is conducted Yes No 4 Has this device been used in a room where testing of infectious diseases is conducted Yes No 5 Has...

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