Directives, Standards And Guidelines; Table A-2: Directives, Standards And Guidelines Sorvall Bios 16 / Sorvall Bios 16 Heavy Duty - Thermo Scientific Sorvall BP 8 Instruction Manual

Thermo Scientific Sorvall BP 8 / 16 and Sorvall BIOS 16 Centrifuges and Heavy Duty Centrifuges

1. Directives, Standards and Guidelines

Centrifuge Region
Thermo Scientific Europe
Sorvall BIOS 16
Single Phase
Thermo Scientific 220, 230 V, 50 / 60 Hz
Sorvall BIOS 16
Poly Phase
Heavy Duty
380, 400, 415 V, 50 Hz
USA & Canada
Single Phase
208, 230, 240 V, 60 Hz
Japan
Single Phase
200 V, 50 / 60 Hz
China
Single Phase
220 V, 50 Hz
Poly Phase
380 V, 50 Hz
Table A–2: Directives, Standards and Guidelines Sorvall BIOS 16 / Sorvall BIOS 16 Heavy Duty
NOTE 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:
ƒ Reorient or relocate the receiving antenna.
Increase the separation between the equipment and receiver.
ƒ
Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
ƒ
Technical Specifications
Directive
2006/42/EC Machinery
2014/35/EU Low Voltage
(Protective Goals)
2014/30/EU Electromagnetic
Compatibility (EMC)
2011/65/EC RoHS
Directive on the Restriction of
the use of certain Hazardous
Substances in electrical and
electronic equipment
FDA listed
Product Code JQC
Centrifuges For Clinical Use
Device Class 1
CFDA listed
A–2
Standard
EN 61010-1
IEC 61010-2-020
EN 61010-2-101
EN 61326-1 Class B
EN 62304
EN 61326-2-6
EN 62366-1
EN ISO 14971
EN ISO 13485
ANSI/UL 61010-1
IEC 61010-2-020
IEC 61010-2-101
IEC 61326-1 Class B
EN 62304
EN 62366-1
EN ISO 14971
EN ISO 13485
FCC Part 15
IEC 61010-1
IEC 61010-2-020
IEC 61010-2-101
IEC 61326-1 Class B
EN 62304
EN 62366-1
EN ISO 14971
EN ISO 13485