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CE Marking

The BUMI Pillow complies with the essential requirements established in Annex I of Directive 93/42 / EEC, of 14 June, in its current wording and Decree-Law no. 145/2009, of 17 June, which apply to them.

Teste 1
Medical Device

The BUMI Pillow is registered at INFARMED (Portuguese National Authority for Medicines and Health Products) as a Class I Medical Device.

Device ID Nr. 162621.

Medical Device 1
Certified Quality System

INTERESPUMA, the manufacturer of BUMI products, is supported by a Quality Management System that allows the sustained development of the company.

INTERESPUMA assumes itself as a reference in the area of Health, governed by a Quality Policy of valorization and continuous improvement under the standard NP EN ISO 9001: 2015.

Certified Quality System 4