Type S030

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2.

Approvals and conformities

2.1. General notes

• The approvals and conformities listed below must be stated when making enquiries. This is the only way to ensure that the product

complies with all required specifications.

• Not all available variants of the device can be supplied with the below mentioned approvals or conformities.

2.2. Conformity

In accordance with the Declaration of Conformity, the product is compliant with the EU Directives.

2.3. Standards

The applied standards which are used to demonstrate compliance with the EU Directives are listed in the EU-Type Examination Certificate

and/or the EU Declaration of Conformity.

2.4. Pressure Equipment Directive (PED)

The device conforms to article 4, paragraph 1 of the Pressure Equipment Directive (PED) 2014/68/EU under the following conditions:

Device used on a pipe

Note:

• The data in the table is independent of the chemical compatibility of the material and the fluid.

• PS = maximum admissible pressure (in bar), DN = nominal diameter of the pipe

Type of fluid

Conditions

Fluid group 1, article 4, paragraph 1.c.i

DN ≤ 25

Fluid group 2, article 4, paragraph 1.c.i

DN ≤ 32 or PS*DN ≤ 1000

Fluid group 1, article 4, paragraph 1.c.ii

DN ≤ 25 or PS*DN ≤ 2000

Fluid group 2, article 4, paragraph 1.c.ii

DN ≤ 200 or PS ≤ 10 or PS*DN ≤ 5000

2.5. Foods and beverages/Hygiene

Note:

The specific sensor fittings (S030-HT) for the measurement of flow rates at high temperature and pressure is not covered by this certificat.

Conformity

Description

FDA

FDA – Code of Federal Regulations (valid for the variable code PL02, PL03)

The variants with the body and the sensor armature made of PVDF or stainless steel materials, the paddle wheel

made of PVDF material and the seal made of FKM or EPDM materials are compliant in their composition with the

Code of Federal Regulations published by the FDA (Food and Drug Administration, USA) according to the manufac-

turer‘s declaration.