NEC MD215MG, Installation & Maintenance Manual

English-2

Registration Information

Declaration

Means of Conformity

Device Classifi cation: 

Class I, non-measuring function

Applicable Rules: 

Annex IX, Rules 1.4 (Section 1)

and 1.1 (Section 3)

Product Name: 

MD215MG

21.3” Diagnostic Imaging LCD Monitor

Model Number: 

MDL2116A

UMDNS Code: 

16-603

NEC Display Solutions Europe GmbH declares that the product 
listed is in conformity with the essential requirements and 
provisions of the Council Directive 93/42/EEC, including the 
amendments of the Council Directive 2007/47/EC, and conforms 
to the applicable clauses of the following standards:

– EN 60601-1

– EN 60601-1-2

– EN 61000-3-2

– EN 61000-3-3

NEC Display Solutions Europe GmbH
Landshuter Allee 12-14. 80637 Muenchen, Germany

Declaration of the Authorized Representative

Declaration of the Authorized Representative

Canadian Department of Communications Compliance Statement

DOC: 

This Class B digital apparatus meets all requirements of the Canadian Interference-Causing Equipment Regulations.

C-UL:

 Bears the C-UL Mark and is in compliance with Canadian Safety Regulations according to CAN/CSA C22.2 No. 601.1.

FCC Information

1.   Use the attached specifi ed cables with the MD215MG grayscale monitor so as not to interfere with radio and television reception.

(1) 

Please use the supplied power cord or equivalent to ensure FCC compliance. 

(2) 

Please use the supplied shielded DVI-D to DVI-D cable. 

Use of other cables and adapters may cause interference with radio and television reception.

2.   This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. 

These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment 
generates, uses, and can radiate radio frequency energy, and, if not installed and used in accordance with the instructions, may cause 
harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. 
If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and 
on, the user is encouraged to try to correct the interference by one or more of the following measures:

•   Reorient or relocate the receiving antenna.
• 

Increase the separation between the equipment and receiver.

• 

Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.

• 

Consult your dealer or an experienced radio/TV technician for help.

If necessary, the user should contact the dealer or an experienced radio/television technician for additional suggestions. 
The user may fi nd the following booklet, prepared by the Federal Communications Commission, helpful: “How to Identify and Resolve 
Radio-TV Interference Problems.” This booklet is available from the U.S. Government Printing Offi ce, Washington, D.C., 20402, 
Stock No. 004-000-00345-4.

Declaration of Conformity

This device complies with Part 15 of FCC Rules. Operation is subject to the following two conditions. (1) This device may not cause harmful 
interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.

U.S. Responsible Party:  NEC Display Solutions of America, Inc.
Address: 

500 Park Boulevard, Suite 1100

  Itasca, 

Illinois 

60143

Tel. 

No.: 

  (630) 

467-3000

Type of Product: 

Display Monitor

Equipment Classifi cation:  Class B Peripheral

Model: MD215MG 

(MDL2116A)

We hereby declare that the equipment specifi ed above conforms 

to the technical standards as specifi ed in the FCC Rules.

Classifi cation

* Type of protection against electric shock: CLASS II equipment
* Degree of protection against electric shock: No applied part
* Degree of protection against ingress of water as detailed in the current edition of IEC529: IPX0 - No protection
* Method of sterilization or disinfection recommended by the manufacturer: Not Specifi ed
* This device is not suitable for use in the presence of a fl ammable Anaesthetic Mixture with Air, Oxygen or Nitrous Oxide: No AP or APG category
* This device shall not be used in the vicinity of the patient, which is the space with surfaces likely to be contacted by the patient or an attendant  
  who can touch the patient. This encloses a space within the room 1.83 m (6 feet) beyond the perimeter of the bed in its intended location, and  
  extending vertically 2.29 m (7-1/ 2 feet) above the fl oor.
* Mode of operation: Continuous operation, maximum 16 hours/7 days