exemptions-art-4-restrictions-rohs

ROHS - Exemptions from Article 4(1) Restrictions, Annexes III & IV

EU. Exemptions from Art. 4(1) Restrictions (Annexes III & IV), Directive 2011/65/EU (RoHS), as amended by Commission Delegated Directive (EU) 2024/232, OJ L of 10 January 2024

This list contains the application exemptions listed in Annexes III and IV to RoHS (2011/65/EU). Annex III contains applications exempted from the restriction in Article 4(1), while Annex IV lists applications exempted from the restriction in Article 4(1) specific to medical devices and monitoring and control instruments.

RELEVANT LEGISLATION
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Last updated 15 travnja 2024. Database contains 242 unique substances/entries.
Substance Name EC No. CAS No. Annex Reference Application Expiration Date  
Bis(2-ethylhexyl) phthalate;DEHP
204-211-0
117-81-7
IV
45
In ion-selective electrodes applied in point of care analysis of ionic substances present in human body fluids and/or in dialysate fluids
07/21/2028
 Details
Bis(2-ethylhexyl) phthalate;DEHP
204-211-0
117-81-7
III
43
In rubber components in engine systems, designed for use in equipment that is not intended solely for consumer use and provided that no plasticised material comes into contact with human mucous membranes or into prolonged contact with human skin and the concentration value of bis(2-ethylhexyl) phthalate does not exceed: (a) 30 % by weight of the rubber for (i) gasket coatings, (ii) solid-rubber gaskets, or (iii) rubber components included in assemblies of at least three components using electrical, mechanical or hydraulic energy to do work, and attached to the engine. (b) 10 % by weight of the rubber for rubber-containing components not referred to in point (a)
07/21/2024
 Details
Bis(2-ethylhexyl) phthalate;DEHP
204-211-0
117-81-7
IV
46
In plastic components in MRI detector coils
01/01/2024
 Details
Bis(2-ethylhexyl) phthalate;DEHP
204-211-0
117-81-7
IV
47
In spare parts recovered from and used for the repair or refurbishment of medical devices, including in vitro diagnostic medical devices, and their accessories, provided that the reuse takes place in auditable closed-loop business-to-business return systems and that each reuse of parts is notified to the customer
07/21/2028
 Details

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