2 Safety

Rating Label Display

The position and contents of the label attached on the CR-2 is shown below.

Follow the information on the label to use the CR-2 appropriately.

The following table describes the marks and indications on the rating label.

Alternating current

Type B

Class I device indicating manufacturer’s declaration of conformance with the Annex VII of the Medical Device Directive, 93/42/EEC

Certification mark that shows the product has passed the tests by

TUV Rheinland of conformity with the medical device regulations in the

European Union.

Product that WEEE directive, Directive on Waste Electrical and Electronic Equipment, 2002/96/EC, requires separate collection. The directive is effective in the European Union only.

Certification mark that indicates the product complies with UL 60601- 1 and CAN/CSA 22.2 No. 601.1, that specifies protection against fire, electric shock, and mechanical hazards

Caution: Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle marked “HOSPITAL GRADE”. This caution applies to the USA only.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.

Year and Month of Production

Example: October 2010

 

 

Serial number in six digits

Example: 123456

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