9.10.2014   

EN

Official Journal of the European Union

C 356/22


Medicinal products — List of marketing authorisations granted by the EEA EFTA States for the first half of 2012

2014/C 356/07

Subcommittee I on the free movement of goods

To be noted by the EEA Joint Committee

With reference to EEA Joint Committee Decision No 74/1999 of 28 May 1999, the EEA Joint Committee is invited to note the following lists concerning marketing authorisations for medicinal products for the period 1 January-30 June 2012, at their meeting on 15 July 2013:

Annex I

List of new marketing authorisations

Annex II

List of renewed marketing authorisations

Annex III

List of extended marketing authorisations

Annex IV

List of withdrawn marketing authorisations

Annex V

List of suspended marketing authorisations


ANNEX I

List of new marketing authorisations

The following marketing authorisations have been granted in the EEA EFTA States during the period 1 January-30 June 2012:

EU-Number

Product

Country

Date of authorisation

EU/1/11/711/001-030

Matever

Norway

1.6.2012

EU/1/11/712/001-028

Levetiracetam Accord

Norway

13.4.2012

EU/1/11/713/001-040

Levetiracetam Actavis

Norway

16.4.2012

EU/1/11/715/001-002

Plenadren

Iceland

23.4.2012

EU/1/11/721/001-021

Paglitaz

Norway

13.4.2012

EU/1/11/721/001-021

Paglitaz

Iceland

17.4.2012

EU/1/11/722/001-030

Pioglitazone Accord

Norway

11.4.2012

EU/1/11/722/001-030

Pioglitazon Accord

Liechtenstein

30.4.2012

EU/1/11/722/001-030

Pioglitazone Accord

Iceland

20.4.2012

EU/1/11/723/001-021

Pioglitazone Krka

Norway

23.5.2012

EU/1/11/723/001-021

Pioglitazone Krka

Iceland

20.4.2012

EU/1/11/727/001

Mercatopurine Nova lab.

Norway

19.4.2012

EU/1/11/727/001

Mercaptopurine Nova Laboratories

Iceland

3.4.2012

EU/1/11/727/001

Mercatopurine Nova Laboratories

Liechtenstein

30.4.2012

EU/1/11/729/001-006

Onduarp

Norway

8.5.2012

EU/1/11/730/001-060

Rasitrio

Iceland

3.2.2012

EU/1/11/738/001-003

Levetiracetam Actavis Gr.

Norway

1.3.2012

EU/1/11/739/001-008

Dasselta

Norway

16.1.2012

EU/1/11/740/001

Ameluz

Iceland

5.1.2012

EU/1/11/740/001

Ameluz

Norway

16.1.2012

EU/1/11/741/001

Levetiracetam SUN

Norway

27.1.2012

EU/1/11/741/001

Levetiracetam Sun

Iceland

9.1.2012

EU/1/11/742/001-010

Efavirenz Teva

Norway

13.2.2012

EU/1/11/742/001-010

Efavirenz Teva

Iceland

24.1.2012

EU/1/11/742/001-010

Efavirenz Teva

Liechtenstein

29.2.2012

EU/1/11/743/001-015

Repaglinide Accord

Norway

13.2.2012

EU/1/11/743/001-015

Repaglinide Accord

Iceland

19.1.2012

EU/1/11/743/001-015

Repaglinide Accord

Liechtenstein

29.2.2012

EU/1/11/744/001-002

Topotecan Eagle

Iceland

22.1.2012

EU/1/11/744/001-002

Topotecan Eagle

Liechtenstein

29.2.2012

EU/1/11/745/001-009

Desloratadine Actavis

Iceland

3.2.2012

EU/1/11/745/001-009

Desloratadine Actavis

Norway

13.2.2012

EU/1/11/746/001-012

Desloratadine ratiopharm

Norway

13.2.2012

EU/1/11/746/001-012

Desloratadine ratiopharm

Iceland

3.2.2012

EU/1/11/746/001-012

Desloratadine ratiopharm

Liechtenstein

29.2.2012

EU/1/11/747/001

Colobreathe

Iceland

29.2.2012

EU/1/11/747/001

Colobreathe

Liechtenstein

29.2.2012

EU/1/11/748/001-006

Docetaxel Mylan

Iceland

7.2.2012

EU/1/11/748/001-006

Docetaxel Mylan

Liechtenstein

29.2.2012

EU/1/11/749/001-002

Caprelsa

Liechtenstein

30.4.2012

EU/1/11/749/001-003

Caprelsa

Iceland

9.3.2012

EU/1/11/749/001-002

Caprelsa

Norway

13.3.2012

EU/1/12/750/001

Esmya

Norway

30.3.2012

EU/1/12/750/001

Esmya

Iceland

14.3.2012

EU/1/12/750/001

Esmya

Liechtenstein

30.4.2012

EU/1/12/751/001

Zelboraf

Norway

14.3.2012

EU/1/12/751/001

Zelboraf

Iceland

7.3.2012

EU/1/12/751/001

Zelboraf

Liechtenstein

29.2.2012

EU/1/12/752/001

Vepacel

Norway

1.3.2012

EU/1/12/752/001

Vepacel

Iceland

9.3.2012

EU/1/12/752/001

Vepacel

Liechtenstein

29.2.2012

EU/1/12/753/001-012

Signifor

Norway

10.5.2012

EU/1/12/753/001-012

Signifor

Iceland

24.5.2012

EU/1/12/753/001-012

Signifor

Liechtenstein

30.6.2012

EU/1/12/754/001-021

Sepioglin

Norway

10.4.2012

EU/1/12/754/001-021

Sepioglin

Iceland

3.4.2012

EU/1/12/754/001-021

Sepioglin

Liechtenstein

30.4.2012

EU/1/12/755/001-027

Pioglitazone Actavis

Norway

13.4.2012

EU/1/12/755/001-027

Pioglitazone Actavis

Iceland

30.4.2012

EU/1/12/756/001-027

Glidipion (ex Ogliton)

Norway

13.4.2012

EU/1/12/756/001-027

Pioglitazone Actavis Group

Iceland

13.4.2012

EU/1/12/756/001-027

Pioglitazone Actavis Group

Liechtenstein

30.4.2012

EU/1/12/757/001-030

Pioglitazone Teva

Norway

11.4.2012

EU/1/12/757/001-030

Pioglitazone Teva

Iceland

23.4.2012

EU/1/12/758/001-030

Pioglitazone Teva Pharma

Norway

17.4.2012

EU/1/12/758/001-030

Pioglitazone Teva Pharma

Iceland

25.4.2012

EU/1/12/759/001-003

Zoledronic acid Actavis

Norway

8.5.2012

EU/1/12/759/001-003

Zoledronic acid Actavis

Iceland

16.5.2012

EU/1/12/759/001-003

Zoledronsäure Actavis

Liechtenstein

30.4.2012

EU/1/12/760/001-002

Bronchitol

Norway

18.5.2012

EU/1/12/760/001-002

Bronchitol

Iceland

9.5.2012

EU/1/12/761/001-002

Capecitabine Teva

Norway

30.5.2012

EU/1/12/761/001-002

Capecitabine Teva

Iceland

20.5.2012

EU/1/12/761/001-002

Capecitabin Teva

Liechtenstein

30.4.2012

EU/1/12/762/001-018

Capecitabine Accord

Iceland

20.5.2012

EU/1/12/762/001-018

Capecitabin Accord

Liechtenstein

30.4.2012

EU/1/12/763/001-018

Capecitabine Krka

Iceland

16.5.2012

EU/1/12/763/001-018

Capecitabin Krka

Liechtenstein

30.4.2012

EU/1/12/763/001-018

Capecitabine Krka

Norway

14.6.2012

EU/1/12/764/001

Pixuvri

Norway

14.6.2012

EU/1/12/764/001

Pixuvri

Iceland

29.5.2012

EU/1/12/764/001

Pixuvri

Liechtenstein

30.6.2012

EU/1/12/765/001-004

Sabervel

Iceland

9.5.2012

EU/1/12/765/001-006

Sabervel

Norway

8.5.2012

EU/1/12/765/001-006

Sabervel

Liechtenstein

30.4.2012

EU/1/12/766/001

Sancuso

Norway

10.5.2012

EU/1/12/766/001

Sancuso

Iceland

20.5.2012

EU/1/12/766/001

Sancuso

Liechtenstein

30.6.2012

EU/1/12/767/001-007

Nimenrix

Norway

1.5.2012

EU/1/12/767/001-007

Nimenrix

Iceland

16.5.2012

EU/1/12/768/001

Riluzole Zentiva

Iceland

25.5.2012

EU/1/12/768/001

Riluzol Zentiva

Liechtenstein

30.6.2012

EU/1/12/769/001-003

Docetaxel Accord

Iceland

12.6.2012

EU/1/12/769/001-003

Docetaxel Accord

Liechtenstein

30.6.2012

EU/1/12/770/001-004

Docetaxel Kabi

Norway

19.6.2012

EU/1/12/770/001-004

Docetaxel Kabi

Iceland

13.6.2012

EU/1/12/770/001-004

Docetaxel Kabi

Liechtenstein

30.6.2012

EU/2/11/134/001-014

Inflacam

Norway

6.1.2012

EU/2/11/135/001-003

Panacur AquaSol

Norway

10.2.2012

EU/2/11/136/001

Truscient

Norway

6.1.2012

EU/2/11/136/001

TruScient

Iceland

12.1.2012

EU/2/11/137/001-015

Activyl Tick Plus

Norway

13.2.2012

EU/2/11/137/001-015

Activyl Tick Plus

Iceland

25.1.2012

EU/2/11/137/001-015

Activyl Tick Plus

Liechtenstein

29.2.2012

EU/2/12/138/001-003

RevitaCAM

Iceland

14.3.2012

EU/2/12/139/001-003

Zulvac 1 + 8 Bovis

Norway

3.4.2012

EU/2/12/139/001-003

Zulvac 1 + 8 Bovis

Iceland

4.4.2012

EU/2/12/139/001-003

Zulvac 1 + 8 Bovis

Liechtenstein

30.4.2012


ANNEX II

List of renewed marketing authorisations

The following marketing authorisations have been renewed in the EEA EFTA States during the period 1 January-30 June 2012:

EU-Number

Product

Country

Date of authorisation

EU/1/01/197/001-005

Foscan

Iceland

14.5.2012

EU/1/01/200/001-002

Viread

Norway

6.1.2012

EU/1/01/200/001-002

Viread

Iceland

5.1.2012

EU/1/02/209/001-008

Dynastat

Norway

8.3.2012

EU/1/02/209/001-008

Dynastat

Iceland

7.2.2012

EU/1/02/209/001-008

Dynastat

Liechtenstein

29.2.2012

EU/1/02/212/001-026

Vfend

Norway

6.3.2012

EU/1/02/212/001-026

Vfend

Iceland

14.3.2012

EU/1/02/212/001-026

Vfend

Liechtenstein

30.4.2012

EU/1/02/216/001-002

Invanz

Norway

19.1.2012

EU/1/02/216/001-002

Invanz

Iceland

20.1.2012

EU/1/02/216/001-002

Invanz

Liechtenstein

29.2.2012

EU/1/02/220/001-006

Tracleer

Norway

8.5.2012

EU/1/02/220/001-006

Tracleer

Iceland

20.5.2012

EU/1/02/220/001-006

Tracleer

Liechtenstein

30.4.2012

EU/1/02/222/001-005

Tamiflu

Norway

8.3.2012

EU/1/02/222/001-005

Tamiflu

Iceland

19.6.2012

EU/1/02/222/001-005

Tamiflu

Liechtenstein

30.6.2012

EU/1/06/334/001-005

Evoltra

Liechtenstein

30.4.2012

EU/1/06/347/001-008

Sutent

Liechtenstein

29.2.2012

EU/1/06/366/005-022

Tandemact

Norway

11.4.2012

EU/1/06/366/005-022

Tandemact

Iceland

22.3.2012

EU/1/06/366/005-022

Tandemact

Liechtenstein

30.4.2012

EU/1/06/367/001-012

Diacomit

Norway

6.3.2012

EU/1/06/367/001-012

Diacomit

Iceland

7.2.2012

EU/1/06/367/001-012

Diacomit

Liechtenstein

29.2.2012

EU/1/06/370/001-039

Exforge

Norway

16.1.2012

EU/1/06/370/001-039

EXFORGE

Iceland

3.2.2012

EU/1/06/371/001-039

Dafiro

Iceland

8.2.2012

EU/1/06/371/001-039

Dafiro

Liechtenstein

29.2.2012

EU/1/06/372/001-039

Copalia

Norway

11.1.2012

EU/1/06/373/001-039

Imprida

Norway

16.1.2012

EU/1/06/373/001-039

Imprida

Iceland

6.2.2012

EU/1/06/374/001

Lucentis

Norway

17.1.2012

EU/1/06/374/001

Lucentis

Iceland

12.1.2012

EU/1/06/376/001-033

Irbesartan Zentiva (ex-Winthrop)

Norway

14.2.2012

EU/1/06/376/001-033

Irbesartan Zentiva

Iceland

7.2.2012

EU/1/06/376/001-033

Irbesartan Winthrop

Liechtenstein

29.2.2012

EU/1/06/377/001-028

Irbesartan HCT Zentiva (ex-Winthrop)

Norway

16.4.2012

EU/1/06/377/001-028

Irbesartan HCT Zentiva

Iceland

22.3.2012

EU/1/06/377/001-028

Irbesartan HCT

Liechtenstein

30.4.2012

EU/1/06/378/001-017

Inovelon

Norway

6.3.2012

EU/1/06/378/001-017

Inovelon

Iceland

24.1.2012

EU/1/06/378/001-017

Inovelon

Liechtenstein

29.2.2012

EU/1/06/379/001

Cystadane

Iceland

9.3.2012

EU/1/06/379/001

Cystadane

Liechtenstein

29.2.2012

EU/1/06/386/001-015, 020-024, 029-033, 038-042, 047-051, 056-057, 088102, 113-150, 163-168

Insulin Human Winthrop

Norway

6.1.2012

EU/1/07/382/001-018

Xelevia

Norway

14.2.2012

EU/1/07/382/001-018

Xelevia

Iceland

6.2.2012

EU/1/07/382/001-018

Xelevia

Liechtenstein

29.2.2012

EU/1/07/383/001-018

Januvia

Norway

26.3.2012

EU/1/07/383/001-018

Januvia

Iceland

11.5.2012

EU/1/07/383/001-018

Januvia

Liechtenstein

30.4.2012

EU/1/07/384/003-005

Docetaxel Winthrop

Norway

10.4.2012

EU/1/07/384/003-005

Docetaxel Winthrop

Iceland

23.3.2012

EU/1/07/384/003-005

Docetaxel Winthrop

Liechtenstein

30.4.2012

EU/1/07/386/001-018

Toviaz

Norway

11.4.2012

EU/1/07/386/001-018

Toviaz

Iceland

10.4.2012

EU/1/07/386/001-018

Toviaz

Liechtenstein

30.4.2012

EU/1/07/387/001-026

Advagraf

Norway

2.5.2012

EU/1/07/387/001-026

Advagraf

Iceland

9.5.2012

EU/1/07/387/001-026

Advagraf

Liechtenstein

30.4.2012

EU/1/07/388/001-003

Sebivo

Norway

8.5.2012

EU/1/07/388/001-003

Sebivo

Iceland

16.5.2012

EU/1/07/388/001-003

Sebivo

Liechtenstein

30.4.2012

EU/1/07/389/001-003

Orencia

Norway

10.4.2012

EU/1/07/389/001-003

Orencia

Iceland

10.4.2012

EU/1/07/389/001-003

Orencia

Liechtenstein

30.4.2012

EU/1/07/390/001-004

Altargo

Norway

8.5.2012

EU/1/07/390/001-004

Altargo

Iceland

16.5.2012

EU/1/07/390/001-004

Altargo

Liechtenstein

30.4.2012

EU/1/07/391/001-004

Revlimid

Norway

3.5.2012

EU/1/07/391/001-004

Revlimid

Iceland

9.5.2012

EU/1/07/391/001-004

Revlimid

Liechtenstein

30.4.2012

EU/1/07/392/001-003

Circadin

Norway

16.5.2012

EU/1/07/392/001-003

Circadin

Iceland

10.5.2012

EU/1/07/392/001-003

Circadin

Liechtenstein

30.6.2012

EU/1/07/394/001-009

Optaflu

Norway

20.6.2012

EU/1/07/395/001-095

Invega

Liechtenstein

30.6.2012

EU/1/07/396/001-003

Pergoveris

Iceland

20.6.2012

EU/1/07/396/001-003

Pergoveris

Liechtenstein

30.6.2012

EU/1/07/398/001-014

Optimark

Norway

27.6.2012

EU/1/07/399/001-006

Aerinaze

Norway

18.6.2012

EU/1/07/399/001-006

Aerinaze

Liechtenstein

30.6.2012

EU/1/07/399/001-006

Aerinaze

Iceland

20.6.2012

EU/1/07/400/008-013, 017-024

Mircera

Iceland

7.6.2012

EU/1/07/400/008-013, 017-024

Mircera

Norway

14.6.2012

EU/1/07/400/017-024

Mircera

Liechtenstein

30.6.2012

EU/1/07/401/007-016

alli

Norway

29.6.2012

EU/1/07/412/001-052

Abseamed

Liechtenstein

30.6.2012

EU/1/07/423/001-003

Vectibix

Norway

19.3.2012

EU/1/07/423/001-003

Vectibix

Iceland

9.3.2012

EU/1/07/440/001-003

Tyverb

Liechtenstein

30.4.2012

EU/1/07/440/001-006

Tyverb

Norway

2.5.2012

EU/1/07/440/001-006

Tyverb

Iceland

11.5.2012

EU/1/10/625/001&003

Arzerra

Iceland

17.2.2012

EU/1/10/625/001&003

Arzerra

Norway

18.5.2012

EU/1/10/628/001-004

Votrient

Norway

19.6.2012

EU/1/10/628/001-004

Votrient

Iceland

13.6.2012

EU/1/11/699/001-004

Fampyra

Norway

19.6.2012

EU/1/11/699/001-004

Fampyra

Iceland

13.6.2012

EU/1/11/699/001-004

Fampyra

Liechtenstein

30.6.2012

EU/2/05/053/001-003

Naxcel

Norway

14.2.2012

EU/2/06/068/001-004

Ypozane

Norway

13.2.2012

EU/2/06/068/001-004

Ypozane

Iceland

18.1.2012

EU/2/06/068/001-004

Ypozane

Liechtenstein

30.4.2012

EU/2/06/070/001-008

Meloxidyl

Iceland

13.1.2012

EU/2/07/071/001-003

SLENTROL

Iceland

7.5.2012

EU/2/07/071/001-003

Slentrol

Liechtenstein

30.4.2012

EU/2/07/072/001-004

Suprelorin

Iceland

21.6.2012

EU/2/07/074/001-006

Prilactone

Iceland

13.6.2012

EU/2/07/075/001-004

Circovac

Liechtenstein

30.6.2012

EU/2/07/075/001-004

Circovac

Iceland

4.6.2012


ANNEX III

List of extended marketing authorisations

The following marketing authorisations have been extended in the EEA EFTA States during the period 1 January-30 June 2012:

EU-Number

Product

Country

Date of authorisation

EU/1/00/141/002

Myocet

Liechtenstein

30.4.2012

EU/1/02/222/05

Tamiflu

Iceland

6.2.2012

EU/1/03/262/009-010

Emend

Norway

5.1.2012

EU/1/03/262/009-010

Emend

Iceland

3.2.2012

EU/1/03/271/007-010

Advate

Norway

23.1.2012

EU/1/03/271/007-010

Advate

Iceland

17.1.2012

EU/1/05/318/003

Revatio

Norway

13.4.2012

EU/1/05/318/003

Revatio

Iceland

17.4.2012

EU/1/05/318/003

Revatio

Liechtenstein

30.4.2012

EU/1/06/339/003

Preotact

Liechtenstein

30.6.2012

EU/1/08/465/021

Clopidogrel Zentiva

Liechtenstein

30.6.2012

EU/1/08/468/002

INTELENCE

Iceland

3.1.2012

EU/1/08/470/018-019

Vimpat

Norway

14.3.2012

EU/1/08/470/018-019

Vimpat

Iceland

14.3.2012

EU/1/08/470/018-019

Vimpat

Liechtenstein

30.4.2012

EU/1/08/472/011-021

Xarelto

Norway

4.1.2012

EU/1/08/475/035-060

Olanzapin Mylan

Liechtenstein

29.2.2012

EU/1/09/536/003-004

Topotecan Actavis

Liechtenstein

30.4.2012

EU/1/09/551/013-027

Vizarsin

Iceland

7.6.2012

EU/1/09/551/013-027

Vizarsin

Liechtenstein

30.6.2012

EU/1/09/571/002

Pandemic influenza vaccine H5N1 Baxter

Liechtenstein

30.4.2012

EU/1/11/667/004

Esbriet

Liechtenstein

30.4.2012

EU/1/11/699/003-004

Fampyra

Liechtenstein

30.4.2012

EU/1/11/701/029-032

Levetiracetam Teva

Liechtenstein

30.6.2012

EU/1/11/703/003

Xgeva

Liechtenstein

29.2.2012

EU/1/11/704/002

Victrelis

Liechtenstein

30.4.2012

EU/1/11/720/002

Incivo

Liechtenstein

30.6.2012

EU/1/97/044/009

Tasmar

Liechtenstein

30.4.2012

EU/2/07/078/015-017

Rheumocam

Norway

13.2.2012

EU/2/07/078/015-017

Rheumocam

Iceland

7.2.2012

EU/2/07/078/015-017

Rheumocam

Liechtenstein

29.2.2012

EU/2/08/085/002-006

Easotic

Liechtenstein

30.4.2012

EU/2/08/090/027

Loxicom

Liechtenstein

30.6.2012

EU/2/10/114/003

Hiprabovis IBR Marker Live

Liechtenstein

29.2.2012

EU/2/97/004/049

Metacam

Liechtenstein

29.2.2012


ANNEX IV

List of withdrawn marketing authorisations

The following marketing authorisations have been withdrawn in the EEA EFTA States during the period 1 January-30 June 2012:

EU-Number

Product

Country

Date of authorisation

EU/1/02/255/001-002

Xigris

Iceland

25.6.2012

EU/1/04/272/001-002

PhotoBarr

Norway

24.5.2012

EU/1/04/272/001-002

Photobarr

Iceland

20.5.2012

EU/1/04/272/001-002

PhotoBarr

Liechtenstein

30.6.2012

EU/1/06/335/001

Valtropin

Iceland

5.6.2012

EU/1/06/335/001

Valtropin

Liechtenstein

30.6.2012

EU/1/06/351/001-003

Livensa

Iceland

11.4.2012

EU/1/06/351/001-003

Livensa

Liechtenstein

30.4.2012

EU/1/06/352/001-003

Intrinsa

Liechtenstein

30.6.2012

EU/1/06/352/001-003

Intrinsa

Iceland

23.6.2012

EU/1/09/534/001-007

Clopidogrel Hexal

Iceland

2.3.2012

EU/1/09/534/001-007

Clopidgrel Hexal

Liechtenstein

29.2.2012

EU/1/09/548/001-007

Clopidogrel Acino Pharma GmbH

Iceland

2.3.2012

EU/1/09/548/001-007

Clopidgrel Acino Pharma GmbH

Liechtenstein

29.2.2012

EU/1/09/549/001-007

Clopidogrel Acino Pharma

Iceland

2.3.2012

EU/1/09/549/001-007

Clopidogrel Acino Pharma

Liechtenstein

29.2.2012

EU/1/10/630/001-002

Docefrez

Iceland

20.6.2012

EU/1/10/630/001-002

Docefrez

Liechtenstein

30.6.2012

EU/1/97/035/003-004

Refludan

Iceland

24.5.2012

EU/1/97/035/001-004

Refludan

Norway

6.6.2012

EU/1/97/035/001-004

Refludan

Liechtenstein

30.6.2012

EU/2/00/028/002-008

Zubrin

Iceland

17.4.2012

EU/2/00/028/002-008

Zubrin

Liechtenstein

30.4.2012

EU/2/03/040/001-002

Gonazon

Norway

2.4.2012

EU/2/03/040/001-002

Gonazon

Iceland

17.4.2012

EU/2/03/040/001-002

Gonazon

Liechtenstein

30.4.2012

EU/2/06/060/001-002

Poulvac FluFend H5N3 RG

Liechtenstein

30.6.2012


ANNEX V

List of suspended marketing authorisations

The following marketing authorisations have been suspended in the EEA EFTA States during the period 1 January-30 June 2012:

EU-Number

Product

Country

Date of authorisation

EU/1/06/361/001-002

Luminity

Iceland

20.6.2012

EU/1/06/361/001-002

Luminity

Liechtenstein

30.6.2012

EU/1/97/037/001

Vistide

Liechtenstein

29.2.2012

EU/1/11/705/001

Vibativ

Iceland

27.6.2012