2009/752/EC: Commission Decision of 12 October 2009 authorising the placing on th... (32009D0752)
EU - Rechtsakte: 13 Industrial policy and internal market

COMMISSION DECISION

of 12 October 2009

authorising the placing on the market of a lipid extract from Antarctic Krill

Euphausia superba

as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council

(notified under document C(2009) 7647)

(Only the English text is authentic)

(2009/752/EC)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Regulation (EC) No 258/97 of the European Parliament and of the Council of 27 January 1997 concerning novel foods and novel food ingredients(1), and in particular Article 7 thereof,
Whereas:
(1) On 29 September 2006 the company Neptune Technologies & Bioressources Inc. made a request to the competent authorities of Finland to place a lipid extract from Antarctic Krill
Euphausia superba
on the market as a novel food ingredient.
(2) On 29 January 2007 the competent food assessment body of Finland issued its initial assessment report. In that report it came to the conclusion that the use of the lipid extract from Antarctic Krill
Euphausia superba
as a food ingredient was acceptable.
(3) The Commission forwarded the initial assessment report to all Member States on 19 February 2007.
(4) Within the 60-day period laid down in Article 6(4) of Regulation (EC) No 258/97 reasoned objections to the marketing of the product were raised in accordance with that provision.
(5) Therefore the European Food Safety Authority (EFSA) was consulted on 31 January 2008.
(6) In the Scientific Opinion of the Panel on dietetic products nutrition and allergies on a request from the European Commission on the safety of lipid extract from
Euphausia superba
as food ingredient, the panel came to the conclusion that the lipid extract from Antarctic Krill
Euphausia superba
was safe under the proposed conditions of use.
(7) On the basis of the initial assessment report, it is established that the lipid extract from Antarctic Krill
Euphausia superba
complies with the criteria laid down in Article 3(1) of the Regulation.
(8) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:

Article 1

Lipid extract from Antarctic Krill
Euphausia superba
as specified in Annex I, may be placed on the market in the Community as a novel food ingredient for the uses and at the maximum levels as listed in Annex II.

Article 2

The designation ‘lipid extract from the crustacean Antarctic Krill
Euphausia superba
’ shall be displayed on the labelling of the product as such or in the list of ingredients of foodstuffs containing it.

Article 3

This Decision is addressed to Neptune Technologies & Bioressources Inc., 225 Promenade du Centropolis, Suite 200, Laval, Quebec H7T 0B3, Canada.
Done at Brussels, 12 October 2009.
For the Commission
Androulla
VASSILIOU
Member of the Commission
(1)  
OJ L 43, 14.2.1997, p. 1
.

ANNEX I

SPECIFICATION OF LIPID EXTRACT FROM ANTARCTIC KRILL

EUPHAUSIA SUPERBA

Description

To produce lipid extract from Antarctic Krill
Euphausia superba
deep-frozen Antarctic krill is crushed and subjected to an extraction with acetone. Proteins and krill material are removed from the lipid extract by filtration. The acetone and residual water are removed by evaporation.

Test

Specification

Saponification value

Not more than 185 mg KOH/g

Peroxide value (PV)

Not more than 0,2 meq O2/kg oil

Moisture and volatiles

Not more than 0,9 %

Phospholipids

Not more than 50 %

Trans-fatty acids

Not more than 1 %

EPA (eicosapentaenoic acid)

Not less than 15 %

DHA (docosahexaenoic acid)

Not less than 7 %

ANNEX II

USES OF LIPID EXTRACT FROM ANTARCTIC KRILL

EUPHAUSIA SUPERBA

Use group

Maximum content of combined DHA and EPA

Dairy products except milk-based drinks

200 mg/100 g or for cheese products 600 mg/100 g

Dairy analogues except drinks

200 mg/100 g or for analogues to cheese products 600 mg/100 g

Spreadable fat and dressings

600 mg/100 g

Breakfast cereals

500 mg/100 g

Food supplements

200 mg per daily dose as recommended by the manufacturer

Dietary foods for special medical purposes

In accordance with the particular nutritional requirements of the persons for whom the products are intended

Foods intended for use in energy restricted diets for weight reduction

200 mg/meal replacement

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