SILVER 400 E

Hazard statements (CLP)

H315, H319, H335

Code

Statements

H315

Causes skin irritation

CLP CLASSIFICATION

CLP]Mixtures/Substances SDS EU 2015 According to Regulation (EU) 2015/830 (REACH Annex II) Skin corrosion/irritation, Category 2 H315 Serious eye damage/eye irritation, Category H319 2 Specific target organ toxicity — Single H335 exposure, Category 3, Respiratory tract irritation

Hazard statements

see section 16 : H315 - Causes skin irritation. H319 - Causes serious eye irritation. H335 - May cause respiratory irritation.

Adverse physicochemical, human health and environmental effects

No additional information available

2.2 Label elements

Labelling according to Regulation (EC) No. 1272/2008 [CLP] Extra labelling to displayExtra classification(s) to display

Hazard pictograms

GHS07

Signal word

Warning

Hazardous Ingredients

Potassium metaborate

Precautionary statements

P261 - Avoid breathing dust/fume/gas/mist/vapours/spray. P271 - Use only outdoors or in a well-ventilated area. P280 - Wear protective gloves/protective clothing/eye protection/face protection. P305+P351+P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P302+P352 - IF ON SKIN: Wash with plenty of water. P501 - Dispose of contents/container to hazardous or special waste collection point, in accordance with local, regional, national and/or international regulation

Other hazards which do not result in classification

Spatter and melting metal can cause burn injuries. UV, IR radiations. Arc ray can severely damage eyes or skin. Formation of dangerous fumes during use. Inhalation of welding fumes may cause respiratory irritation. Excessive or prolonged inhalation of fumes may cause metal fever. Hazardous decomposition products may be released during prolonged heating like smokes, carbon monoxide and dioxide, NOx. Electric shocks can kill. Persons with a pacemaker should not go near welding or cutting operations until they have consulted their doctor and obtained information from the manufacturer of the device.