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Certifications

ISO 9001:2000
ISO 9001 has become an international reference for quality management requirements in business-to-business dealings

CERTIFICATE REGISTRATION NO.: SY 60012940 0001
REPORT NO.: 16700332 001
VALID UNTIL: 2010-12-04
VIEW CERTIFICATE
ISO 13485:2003
The certification of a quality management system, specifically for medical devices, to ISO 9001/ISO 13485(EN 46001)proves advantageous, and in many cases essential, for medical companies which export their products to the global market.

CERTIFICATE REGISTRATION NO.: SX 60012939 0001
REPORT NO.: 16700332 001
VALID UNTIL: 2010-12-04
VIEW CERTIFICATE
CE
CE Marking is legally required (mandatory) for products intended for sale or placed into service in Europe. CE Marking covers an estimated 75% of all products sold today in the EU. The requirements for CE Marking apply to all manufacturers, whether located within or outside of the EU.

REGISTRATION NO.: DD 60012938 0001
REPORT NO.: 16700332 001
VALID UNTIL: 2010-12-04
VIEW CERTIFICATE