Plum Eye Wash
Relevant identified uses of the substance or mixture and uses advised against
Recommended uses: Eye wash.
Rinsing of foreign bodies and chemicals from the eyes.
Description of first aid measures
Inhalation: The product does not release hazardous vapours.
Ingestion: Seek medical advice in case of discomfort.
Skin contact: Seek medical advice in case of persistent discomfort.
Eye contact: Not applicable.
General: The product is intended for first aid, and its use should always be followed by a visit to the doctor. If defects or adverse side effects are found during use, please report such defects or side effects to Plum A/S, info@plum.dk by phone +45 6471 2112, so that the necessary remedies can be initiated and the obligation to report serious adverse effects according to Appendix VII item 4 of the Directive can be observed. Serious adverse effects should always be reported to the Board of Health in the state in which the side effect has occurred.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
The product is a medical device covered by Council Directive 93/42/EEC on medical devices. Consequently, the product does not require a safety data sheet and therefore this data sheet does not fully meet the statutory requirements for a safety data sheet.
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