1. 6’-sialyllactose (‘6’-SL’) sodium salt as specified in the Annex to this Regulation shall be included in the Union list of authorised novel foods established in Implementing Regulation (EU) 2017/2470.
2. For a period of 5 years from the date of entry into force of this Regulation only the initial applicant:
Company: Glycom A/S;
Address: Kogle Allé 4, DK-2970 Hørsholm, Denmark,
is authorised to place on the market within the Union the novel food referred to in paragraph 1, unless a subsequent applicant obtains authorisation for that novel food without reference to the data protected pursuant to Article 2 or with the agreement of the applicant.
3. The entry in the Union list referred to in paragraph 1 shall include the conditions of use and labelling requirements laid down in the Annex.
The data contained in the application file on the basis of which 6’-sialyllactose sodium salt has been assessed by the Authority, claimed by the applicant as fulfilling the requirements laid down in Article 26(2) of Regulation 2015/2283, shall not be used for the benefit of any subsequent applicant for a period of 5 years from the date of entry into force of this Regulation without the agreement of the applicant.
The Annex to Implementing Regulation (EU) 2017/2470 is amended in accordance with the Annex to this Regulation.
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union.
ANNEXSupplementary provisions
ANNEX
The Annex to Implementing Regulation (EU) 2017/2470 is amended as follows:
(1)
in Table 1 (Authorised novel foods), the following entry is inserted in alphabetical order:
‘ Authorised novel food
Conditions under which the novel food may be used
Additional specific labelling requirements
Other requirements
Data Protection
6’-Sialyllactose (6’-SL) sodium salt
(microbial source)
Specified food category
Maximum levels (expressed as 6’-Sialyllactose)
The designation of the novel food on the labelling of the foodstuffs containing it shall be “6’-Sialyllactose sodium salt”.
The labelling of food supplements containing 6’-Sialyllactose (6’-SL) sodium salt shall bear a statement that they should not be consumed:
a)
if foods containing added 6’-Sialyllactose sodium salt are consumed on the same day.
b)
by infants and young children
Authorised on 17 February 2021. This inclusion is based on proprietary scientific evidence and scientific data protected in accordance with Article 26 of Regulation (EU) 2015/2283.
Applicant: Glycom A/S, Kogle Allé 4, DK-2970 Hørsholm, Denmark. During the period of data protection, the novel food 6’-sialyllactose sodium salt is authorised for placing on the market within the Union only by Glycom A/S, unless a subsequent applicant obtains authorisation for the novel food without reference to the proprietary scientific evidence or scientific data protected in accordance with Article 26 of Regulation (EU) 2015/2283 or with the agreement of Glycom A/S.
End date of the data protection: 17 February 2026.’
Unflavoured pasteurised and unflavoured sterilised (including UHT) milk products
0,5 g/L
Unflavoured fermented milk-based products
0,5 g/L (beverages)
2,5 g/kg (products other than beverages)
Flavoured fermented milk-based products including heat-treated products
0,5 g/L (beverages)
5,0 g/kg (products other than beverages)
Beverages (flavoured drinks, excluding drinks with a pH less than 5)
0,5 g/L
Cereal bars
5,0 g/kg
Infant formula as defined under Regulation (EU) No 609/2013
0,4 g/L in the final product ready for use, marketed as such or reconstituted as instructed by the manufacturer
Follow-on formula as defined under Regulation (EU) No 609/2013
0,3 g/L in the final product ready for use, marketed as such or reconstituted as instructed by the manufacturer
Processed cereal-based food and baby food for infants and young children as defined under Regulation (EU) No 609/2013
0,3 g/L (beverages) in the final product ready for use, marketed as such or reconstituted as instructed by the manufacturer
2,5 g/kg for products other than beverages
Milk based drinks and similar products intended for young children
0,3 g/L (beverages) in the final product ready for use, marketed as such or reconstituted as instructed by the manufacturer
Total diet replacement foods for weight control as defined under Regulation (EU) No 609/2013
1,0 g/L (beverages)
10,0 g/kg (products other than beverages)
Food for special medical purposes as defined under Regulation (EU) No 609/2013
In accordance with the particular nutritional requirements of the persons for whom the products are intended
Food Supplements as defined in Directive 2002/46/EC, excluding food supplements for infants and young children
1,0 g/day
(2)
in Table 2 (Specifications), the following entry is inserted in alphabetical order:
‘ Authorised Novel Food
Specification
6’-Sialyllactose (“6’-SL”) sodium salt
(microbial source)
Description:
6’-Sialyllactose (6’-SL) sodium salt is a purified, white to off-white powder or agglomerate that is produced by a microbial process and contains limited levels of lactose, 6’-sialyl-lactulose, and sialic acid.
Source: Genetically modified strain of Escherichia coli K-12 DH1
Definition:
Chemical formula: C 23 H 38 NO 19 Na
Chemical name: N-Acetyl-α-D-neuraminyl-(2→6)-β-D-galactopyranosyl-(1→4)-D-glucose, sodium salt
Molecular mass: 655,53 Da
CAS No 157574-76-0
Characteristics/Composition:
Appearance: White to off-white powder or agglomerate
Sum of 6’-Sialyllactose sodium salt, D-Lactose and Sialic acid (% of dry matter): ≥ 94,0 % (w/w)
6’-Sialyllactose sodium salt (% of dry matter): ≥ 90,0 % (w/w)
D-Lactose: ≤ 5,0 % (w/w)
Sialic acid: ≤ 2,0 % (w/w)
6’-Sialyl-lactulose: ≤ 3,0 % (w/w)
Sum of other carbohydrates: ≤ 3,0 % (w/w)
Moisture: ≤ 6,0 % (w/w)
Sodium: 2,5-4,5 % (w/w)
Chloride: ≤ 1,0 % (w/w)
pH (20 °C, 5 % solution): 4,5-6,0
Residual protein: ≤ 0,01 % (w/w)
Microbiological criteria:
Aerobic mesophilic bacteria total plate count: ≤ 1 000 CFU/g
Enterobacteriaceae : ≤ 10 CFU/g
Salmonella sp.: Absence in 25 g
Yeast: ≤ 100 CFU/g
Mould: ≤ 100 CFU/g
Residual endotoxins: ≤ 10 EU/mg
CFU: Colony Forming Units; EU: Endotoxin Units.’
