Fusedrawer 2

Detailed information on product approvals, code requirements, usage instructions and detailed test conditions can be looked up in  Details about Approvals
SCHURTER products are designed for use in industrial environments. They have approvals from independent testing bodies according to national and international standards. Products with specific characteristics and requirements such as required in the automotive sector according to IATF 16949, medical technology according to ISO 13485 or in the aerospace industry can be offered exclusively with customer-specific, individual agreements by SCHURTER.

Application standards

Application standards where the product can be used

Organization	Design	Standard	Description
	Suitable for applications acc.	IEC/UL 62368-1	Audio/video, information and communication technology equipment - Part 1: Safety requirements
	Suitable for applications acc.	IEC 60601-1	Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
	Suitable for applications acc.	IEC 60335-1	Safety of electrical appliances for household and similar purposes. Meets the requirements for appliances in unattended use. This includes the enhanced requirements of glow wire tests acc. to IEC 60695-2-11 or -12 & -13.

Compliances

The product complies with following Guide Lines

Identification	Details	Initiator	Description
	RoHS	SCHURTER AG	Directive RoHS 2011/65/EU, Amendment (EU) 2015/863
	China RoHS	SCHURTER AG	The law SJ / T 11363-2006 (China RoHS) has been in force since 1 March 2007. It is similar to the EU directive RoHS.
	REACH	SCHURTER AG	On 1 June 2007, Regulation (EC) No 1907/2006 on the Registration, Evaluation, Authorization and Restriction of Chemicals 1 (abbreviated as "REACH") entered into force.
	White Paper Glow wire test	SCHURTER AG	Meets the requirements of IEC 60335-1 for appliances in unattended use. This includes the enhanced requirements of glow wire tests acc. to IEC 60695-2-11 or -12 &-13.
	Medical Equipment	SCHURTER AG	Suitable for use in medical equipment according to IEC/UL 60601-1 (1 MOOP, 1 MOPP)