Pendant Technical Specification for Operating Room

ANESTHESIA PENDANT:

The movable pendant arm, which we call the anesthesia pendant, should have the following features.

The movable pendant arm should be moved approximately 600 mm with the electric motor and should be parked at the desired point.

Movable pendant arm 90 kg. It must be capable of bearing weight.

The movable pendant arm should be able to rotate 340° around its own axis.

The Movable Pendant Arm should be terminated on the suspended ceiling with a square steel flange and adapters that can be connected to the ceiling with the NIST connection system defined separately for each gas.

Medical Gases and Vacuum System AntiStatic, brought with Copper Pipes, must be connected to the pandants with pressed special hoses manufactured in accordance with EN 739:1998 norm, with NIST connection at the ends. The name of the relevant gas must be permanently written on the hose.

-Moving Pendant Arm ceiling connection will be covered with a cover painted in RAL 9002 color on the suspended ceiling.

Anesthesia pendant, double-plate console should be available. The console should have a height of 650 mm and 2 tables of 500x470x25 mm on it and 30×10 mm stainless steel hanger rails on the side. Console side profiles should have round radius and should have channels for device fastening.

The following services should be present on the console.

2 pcs Oxygen gas outlet,

1 pcs nitrous oxide gas outlet,

1 pcs Medical air 4 bar gas socket,

2 pcs Medical Vacuum gas sockets,

1 x Anesthesia Gas waste gas socket,

2 pcs Electrical Module box, 4 in each

a total of 8 grounded electrical sockets,

Electrical Module Boxes must be manufactured from plastic by injection method and painted over.

1 AGSS pump start switch,

2 device hanger rails on the sides,

 

All operating room pendants will be painted with RAL 9002 Electrostatic Powder.

 

The product must be CE certified according to the European Medical Devices directive 93/42/EEC. Within the scope of the document, the product must be written.

 

The Manufacturer and Founder Company must have IS9001 and EN 46001 Quality certificates.

SURGICAL PENDANT:

 

The movable pendant arm, which we call the surgical pendant, should have the following features.

The movable pendant arm should be moved approximately 600 mm with the electric motor and should be parked at the desired point.

Movable pendant arm 90 kg. It must be capable of bearing weight.

The movable pendant arm should be able to rotate 340° around its own axis.

The Movable Pendant Arm should be terminated on the suspended ceiling with a square steel flange and adapters that can be connected to the ceiling with the NIST connection system defined separately for each gas.

Medical Gases and Vacuum System AntiStatic, brought with Copper Pipes, must be connected to the pandants with pressed special hoses manufactured in accordance with EN 739:1998 norm, with NIST connection at the ends. The name of the relevant gas must be permanently written on the hose.

Movable Pendant Arm ceiling connection will be covered with a cover painted in RAL 9002 color on the suspended ceiling.

It should have a surgical pendant and a console with double tables. The console should have 650 mm height and 2 tables of 500x470x25 mm on it and 30×10 mm stainless steel hanger rails on the side. Console side profiles should have round radius and should have channels for device mounting.

The following services should be present on the console.

2 pcs Oxygen gas outlet,

1 pcs nitrous oxide gas outlet,

1 pcs Medical air 4 bar gas outlet, BS

2 pcs Medical Vacuum gas sockets,

1 pcs Anesthesia Gas waste gas socket,

2 pcs Electrical Module boxes, 4 in each

a total of 8 grounded electrical sockets,
Electrical Module Boxes must be manufactured from plastic by injection method and painted over.

1 pcs AGSS pump start switch,

2 pcs device hanger rails on the sides,

 

All operating room pendants will be painted with RAL 9002 Electrostatic Powder.

 

The product must be CE certified according to the European Medical Devices directive 93/42/EEC. The Product must be written within the scope of the document.

 

The Manufacturer and Founder Company must have IS9001 and EN 46001 Quality certificates.