Arti-Cell Forte (--) Suspension for injection
Arti-Cell Forte (--) Suspension for injection
Authorised
- Equine allogeneic peripheral blood-derived chondrogenic induced mesenchymal stem cells
Product identification
Medicine name:
Arti-Cell Forte (--) Suspension for injection
Active substance:
- Equine allogeneic peripheral blood-derived chondrogenic induced mesenchymal stem cells
Target species:
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Horse
Route of administration:
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Intraarticular use
Product details
Active substance and strength:
-
Equine allogeneic peripheral blood-derived chondrogenic induced mesenchymal stem cellsPresentation_strength:1.4 to 2.5 x 10⁶ cells Reference:Hse Index:0
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intraarticular use
- Horse
-
Not applicable0dayZero days
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM09AX90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
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Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
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Liechtenstein
-
Lithuania
-
Luxembourg
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Malta
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Netherlands
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Norway
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Poland
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Portugal
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Romania
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Slovakia
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Slovenia
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Spain
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Sweden
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United Kingdom (Northern Ireland)
Package description:
- Packaging:Suspension (stem cells): vial (COC); Suspension (plasma): vial, Package_size:1 vial of stem cell suspension + 1 vial of plasma suspension, Content:Suspension (stem cells): 1 ml; Suspension (plasma): 1 ml
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Global Stem cell Technology
Responsible authority:
- European Commission
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 6/11/2022
Bulgarian (PDF)
Published on: 6/11/2022
Croatian (PDF)
Published on: 6/11/2022
Czech (PDF)
Published on: 6/11/2022
Danish (PDF)
Published on: 6/11/2022
Dutch (PDF)
Published on: 6/11/2022
Estonian (PDF)
Published on: 6/11/2022
Finnish (PDF)
Published on: 6/11/2022
French (PDF)
Published on: 6/11/2022
German (PDF)
Published on: 6/11/2022
Greek (PDF)
Published on: 6/11/2022
Hungarian (PDF)
Published on: 6/11/2022
Icelandic (PDF)
Published on: 6/11/2022
Italian (PDF)
Published on: 6/11/2022
Latvian (PDF)
Published on: 6/11/2022
Lithuanian (PDF)
Published on: 6/11/2022
Maltese (PDF)
Published on: 6/11/2022
Norwegian (PDF)
Published on: 6/11/2022
Polish (PDF)
Published on: 6/11/2022
Portuguese (PDF)
Published on: 6/11/2022
Romanian (PDF)
Published on: 6/11/2022
Slovak (PDF)
Published on: 6/11/2022
Slovenian (PDF)
Published on: 6/11/2022
Spanish (PDF)
Published on: 6/11/2022
Swedish (PDF)
Published on: 6/11/2022
ema-puar-arti-cell-fortev-4727-par-en.pdf
English (PDF)
Download Published on: 1/02/2023
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